Category: 14258-40-3

Computed Properties of C6H11ClO3On May 6, 2016 ,《Synthesis Toward and Stereochemical Assignment of Clathsterol: Exploring Diverse Strategies to Polyoxygenated Sterols》 appeared in Organic Letters. The author of the article were Zhou, Tao; Feng, Feng; Shi, Yong; Tian, Wei-Sheng. The article conveys some information:

Herein we describe a synthesis of the trisulfate derivative I of clathsterol (II), a marine sterol endowed with impressive structural features and moderate inhibitory activity against HIV-1 reverse transcriptase. By synthesizing two possible isomers of the side chain, the stereochem. of II is assigned. In creating chiral side chains from steroidal lactone, our strategies, including an addition/reduction procedure to give C22R-OH, an epoxide-opening reaction, and a [3.3]-rearrangement to induce the generation of C24S-Et and C24R-Et resp., are highly flexible and complementary to each other. After reading the article, we found that the author used 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Computed Properties of C6H11ClO3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Computed Properties of C6H11ClO3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

El Ashry, E. S. H.; Abdel-Rahman, A. A.-H.; Rashed, N.; Rasheed, H. A. published their research in Pharmazie on December 31 ,1999. The article was titled 《Homoacyclovir analogs of unnatural bases and their activity against hepatitis B virus》.HPLC of Formula: 14258-40-3 The article contains the following contents:

The ambident nucleophilic nature of the sodium salts of 2(1H)-quinoxalinone and 2-phenylphthalazinedione has been realized from their alkylation with 2-(2-chloroethoxy)ethyl acetate to afford N- and O-alkylated derivatives, e.g., I and II. Four addnl. N-alkylated heterocycles were similarly prepared from unnatural bases. Treatment of the alkylated derivatives with methanolic ammonia solution (1:1) at room temperature gave the hydroxyalkyl derivatives The site of alkylation was deduced from the spectral characteristics of the products. The activity of several compounds against hepatitis B virus in HepG2 cells has been tested. Some of the compounds showed high viral replication inhibition with low cytotoxicity. In the experiment, the researchers used many compounds, for example, 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3HPLC of Formula: 14258-40-3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.HPLC of Formula: 14258-40-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The author of 《Heavier chalcogenone complexes of bismuth(III)trihalides: potential catalysts for acylative cleavage of cyclic ethers》 were Srinivas, Katam; Suresh, Paladugu; Babu, Chatla Naga; Sathyanarayana, Arruri; Prabusankar, Ganesan. And the article was published in RSC Advances in 2015. Computed Properties of C6H11ClO3 The author mentioned the following in the article:

Heavier chalcogenones (S, Se and Te) of imidazole act as versatile ligands to yield a series of mononuclear and dinuclear bismuth(III)complexes of heavier chalcogenones in excellent yield. These new bismuth heavier chalcogen derivatives are the first structurally characterized mols., where the bismuth and heavier chalcogen ratio is 1 : 1. There is only one previous report of a crystal structure of a bismuth(III)-imidazol selone compound and none with bismuth(III)-imidazol tellone. The bismuth center in monomeric bismuth chalcogen trihalides depicts pseudo trigonal bipyramidal geometry, while the dimeric bismuth chalcogen trihalides demonstrate distorted square pyramidal geometry. The solid state structures of bismuth chalcogenone derivatives feature rare Bi···π(aryl) interactions. Thus, the centroid of the C6-ring suggests a half sandwich type of bismuth environment in mononuclear and dinuclear bismuth(III) chalcogenone complexes. Notably, the Bi···π(aryl) interaction is not often noticed for mononuclear bismuth chalcogen compounds Some of the bismuth(III) chalcogenone complexes also exhibit C-H···π(aryl), C-H···S and C-H···Cl types of hydrogen bonding. The bismuth-chalcogen bond distance in mononuclear bismuth(III) tribromide chalcogenone complexes is slightly longer than in mononuclear bismuth(III) trichloride chalcogenone complexes. A gradual increase in carbon-chalcogen bond distance was observed from the free imidazole-chalcogenone to mononuclear bismuth(III) trichloride chalcogenones, dinuclear bismuth(III) trichloride chalcogenones and mononuclear bismuth(III) tribromide chalcogenones and dinuclear bismuth(III) tribromide chalcogenones. The UV-vis absorption properties and thermal decomposition properties of imidazol chalcogenones and their bismuth derivatives were investigated. Furthermore, the O-acylative cleavage of cyclic ethers was demonstrated using mononuclear and dinuclear bismuth(III) complexes of heavier chalcogenones as catalysts. In contrast to bismuth(III) trichloride and bismuth(III) tribromide catalysts, mononuclear and dinuclear bismuth(III) complexes of heavier chalcogenones are very active towards an acylative cleavage of cyclic ethers through a mild and regioselective strategy. In particular, mononuclear imidazolthione-bismuth(III) trichloride is very active towards O-acylative cleavage of 2-Me THF. The experimental part of the paper was very detailed, including the reaction process of 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Computed Properties of C6H11ClO3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Computed Properties of C6H11ClO3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

In 2017,ChemPlusChem included an article by Champagne, Pier-Luc; Ester, David; Ward, Sandra; Williams, Vance E.; Ling, Chang-Chun. Related Products of 14258-40-3. The article was titled 《A family of amphiphilic cyclodextrin liquid crystals governed by dipole-dipole interactions》. The information in the text is summarized as follows:

A novel family of amphiphilic cyclodextrin (CD)-based liquid crystals that bear O-acetylated oligoethylene glycol chains at the secondary face is reported. Unlike most of the previously reported liquid crystals (LC) based on chem. modified CDs, which depend on H-bonding as the primary intermol. forces, the present CD derivatives self-assemble into highly ordered smectic liquid crystal phases via the weaker dipole-dipole intermol. interactions. The obtained materials are found to display much improved properties such as improved thermostability, reduced clearing temperatures, and better fluidity. The present work opens up new possibilities to design CD-based LC materials. In the experimental materials used by the author, we found 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Related Products of 14258-40-3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Related Products of 14258-40-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

《Effect of alkyl substitution in drugs. XVII. Synthesis on pharmacological properties of alkyl-substituted benzhydryl derivatives of piperazine》 was written by Gootjes, J.; Funcke, A. B. H.; Tersteege, H. M.; Nauta, Wijbe T.. Product Details of 14258-40-3 And the article was included in Arzneimittel-Forschung in 1966. The article conveys some information:

Benzhydryl piperazin-2-ylmethyl ethers, benzhydryl 2-(4-phenylpiperazino)ethyl ethers, benzhydryl 2-(2-piperazinoethoxy)ethyl ethers, and bis(benzhydryl ethers) of 1,4-bis(hydroxyethoxyethyl)piperazines are prepared Benzhydryl 1,4-dimethylpiperazin-2-ylmethyl ether (I) shows papaverine-like action on isolated guinea pig ileum. The compounds prepared are (b.p./mm. and m.p. given): 1,4-bis(p-toluenesulfonyl)-2-piperazinemethanol, -, 174-5°; 2-piperazinemethanol, 140-1°/15, – (maleate m. 149.5-50°); 1,4-dimethyl-2-piperazinemethanol (II), 102-4°/15, -, (maleate m. 144-6°); 4-diphenylmethyl-1-phenylpiperazine, -, -; ClCH2CH2OCH2CH2OAc, 97°/10, -; 2-(2-piperazinoethoxy)ethanol, 150-5°/2, – (maleate m. 121.5-3°); 2-[2-(4-methylpiperazino)ethoxy]ethanol, 115-20°/2, – (HCl salt m. 213-15°); 2,2′-[1,4-piperazinediylbis(ethyleneethoxy)]diethanol, 180-210°/0.1, – (HCl salt m. 179-81°); trans-2,2′-[2,5-dimethyl-1,4-piperazinediylbis(ethyleneoxy)]diethanol, 192-6°/3, 57-60°. A mixture of Ph2CHOH, II, and K2CO3 is heated 1 hr. at 180° to give 47% I di-oxalate, m. 185.5-6°. Similarly prepared are (m.p. and % yield given): o-methylbenzhydryl 1,4-dimethylpiperazin-2-ylmethyl ether di-oxalate hydrate, 119-20°, 31; o-tert-butylbenzhydryl, 1,4-dimethylpiperazin-2-ylmethyl ether di-oxalate, 184.5-5°, 27; III (n = 0, R1 = R2 = R3 = R4 = R5 = R6 = R8 = H), 125-6°, 49; the following III (n = 1, R7 = OCH2CH2)(R1, R2, R3, R4, R5, R6, R8, m.p., and salt m.p. given): H, H, H, H, H, H, H, -, oxalate hemihydrate 177-9°; Me, H, H, H, H, H, H, -, oxalate hemihydrate 162-3°; H, MeO, H, H, MeO, H, H, -, hemioxalate 197-8°; Me, H, Me, Me, H, Me, H, 98-9°, -; H, H, H, H, H, H, Me, -, HCl 153-4°; the following IV (R1, R2, R3, R4, R5, R6, R7, R8, and salt m.p. given): H, H, H, H, H, H, H, Me, 2HCl 179-81.5°; Me, H, H, H, H, H, H, Me, 2HCl 180-2°; H, Me, H, H, H, H, H, Me, 2HCl 137-9°; Me, H, Me, Me, Me, H, H, Me, -; Et, H, Et, Et, Et, H, H, Me, -; H, H, H, H, H, Me, Me, Me, 2HCl 177-9° (trans); Me, H, H, H, H, Me, Me, Me, 2HCl 167-8.5° (trans); H, H, H, H, H, H, H, O(CH2CH2O)2H, dimaleate 137.5-9°; Me, H, H, H, H, H, H, O(CH2CH2O)2H, dimaleate 138.5-40°; Me, H, Me, Me, Me, H, H, O(CH2CH2O)2H, dimaleate 143-4°; the following V (R1, R2, R3, R4, and m.p. salt given): tert-Bu, H, H, H, dimaleate 150-1.5°; Me, Me, H, H, dimaleate 153.5-5°; H, H, Me, Me, 2HCl 186-7.5° (trans); Me, H, Me, Me, 2HCl 182-3° (trans). In the part of experimental materials, we found many familiar compounds, such as 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Product Details of 14258-40-3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Product Details of 14258-40-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

《Synthesis by addition across C-O bonds》 was published in Science of Synthesis in 2007. These research results belong to Rueck-Braun, K.; Freysoldt, T.. Reference of 2-(2-Chloroethoxy)ethyl acetate The article mentions the following:

A review of methods to prepare functionalized organochlorine derivatives with both chloro and secondary functionality generated simultaneously by addition reactions across carbon oxygen bonds. Specifically, the review covers ring opening reactions of oxiranes and cyclic ethers. The results came from multiple reactions, including the reaction of 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Reference of 2-(2-Chloroethoxy)ethyl acetate)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Reference of 2-(2-Chloroethoxy)ethyl acetate

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

The author of 《Soft lithography on block copolymer films: Generating functionalized patterns on block copolymer films as a basis to further surface modification》 were Brehmer, Martin; Conrad, Lars; Funk, Lutz; Allard, Dirk; Theato, Patrick; Helfer, Anke. And the article was published in ACS Symposium Series in 2004. Synthetic Route of C6H11ClO3 The author mentioned the following in the article:

Functionalized patterns on the surfaces of amphiphilic diblock copolymer films were generated using polar/apolar interactions applied by soft lithog. techniques. Further modification of the patterned surfaces included e.g. the deposition of conducting and semiconducting material, which offers the opportunity to build sensor structures ranging from the micron to the submicron size. After reading the article, we found that the author used 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Synthetic Route of C6H11ClO3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Synthetic Route of C6H11ClO3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

《Increments of the arithmetic retention index for polyoxyethylene glycol monoalkyl ethers and their degradation products》 was written by Szymanowski, J.; Kusz, P.; Szewczyk, H.. Recommanded Product: 14258-40-3 And the article was included in Journal of Chromatography on August 30 ,1989. The article conveys some information:

The arithmetic retention indexes for CmH2m+1O(CH2CH2O)nH (m = 12, 14, 16, 18; n = 0-8) were calculated for OV 101 and Dexsil 400 columns, with average absolute and relative errors of 10 and 0.5%, resp. Chlorinated and ester degradation products were similarly assessed. The experimental part of the paper was very detailed, including the reaction process of 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Recommanded Product: 14258-40-3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Recommanded Product: 14258-40-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Abdel-Megied, Ahmed E. S.; Pedersen, Erik B.; Nielsen, Carsten M. published their research in Chemica Scripta on December 31 ,1989. The article was titled 《Synthesis and biological activity of 1-(5-hydroxy-3-oxapentyl)- and 1-(8-hydroxy-3,6-dioxaoctyl)uracils》.SDS of cas: 14258-40-3 The article contains the following contents:

Title compounds I (R = H, Me, CH2OCH2Ph, F, NO2; R1 = H; n = 2, 3) and II (R = Me, CH2OCH2Ph, R1 = H) were prepared by treating uracils III with NaH and Cl(CH2CH2O)nCOMe and then ammonolysis of I and II (R1 = Ac) with NH3-MeOH. A screen of selected compounds, including cytosine IV prepared from I (R = H, R1 = Ac, n = 2), for virucidal activity against herpes simplex virus type 1 and human immunodeficiency virus type 1 showed no significant activity. In the experiment, the researchers used many compounds, for example, 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3SDS of cas: 14258-40-3)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.SDS of cas: 14258-40-3

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics

Zeid, Ibrahim F.; Abdel-Rahman, Adel A.-H.; Abdel-Megied, Ahmed E.-S.; El-Etrawy, Abd-Allah Sh. published an article on January 31 ,1999. The article was titled 《Synthesis of new thiolated acyclonucleosides with potential anti-HBV activity》, and you may find the article in Nucleosides & Nucleotides.Safety of 2-(2-Chloroethoxy)ethyl acetate The information in the text is summarized as follows:

Treatment of the sodium salt of 2-alkylthio-pyrimidin-4(1H)-ones with chloroethyl Me ether, 2-chloroethyl toluoylate or 2-(2-chloroethoxy)ethyl acetate afforded the corresponding derivatives Ammonolysis of at room temperature gave the corresponding hydroxyalkyl derivatives Alkylation of 2,4-dithiouracil gave 2,4-dialkylthio pyrimidine. Several compounds exhibited antiviral activity and cytotoxicity. The experimental part of the paper was very detailed, including the reaction process of 2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3Safety of 2-(2-Chloroethoxy)ethyl acetate)

2-(2-Chloroethoxy)ethyl acetate(cas: 14258-40-3) belongs to aliphatic hydrocarbons. Aliphatic hydrocarbons belong to the most abundant fraction in crude oil. Aliphatics molecules are linear or branched open-chain structures such as n-alkanes, isoalkanes, cycloalkanes (naphthenes), terpenes and steranes.Safety of 2-(2-Chloroethoxy)ethyl acetate

Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics