Category: 6294-17-3

Intramolecular Nucleophilic Substitution of ω-Haloalkylphosphine Derivatives was written by Woznicki, Pawel;Korzeniowska, Ewelina;Stankevic, Marek. And the article was included in Journal of Organic Chemistry in 2017.Electric Literature of C6H12BrCl The following contents are mentioned in the article:

ω-Haloalkylphosphine derivatives undergo the intramol. nucleophilic substitution reaction upon treatment with a strong base, yielding either cycloalkylphosphine derivatives or heterocyclic phosphine derivatives The selectivity of the cyclization of (ω-haloalkyl)alkylarylphosphine derivatives depends strongly on the distance between the electrophilic and nucleophilic C atoms and the structure of the P moiety. The desymmetrization of dimethylphenylphosphine sulfide followed by haloalkylation and cyclization led to the enantiomerically enriched tertiary phosphine sulfide, possessing a cyclohexyl fragment at the P. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Electric Literature of C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Electric Literature of C6H12BrCl

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

Enantiomerically Enriched Tris(boronates): Readily Accessible Conjunctive Reagents for Asymmetric Synthesis was written by Coombs, John R.;Zhang, Liang;Morken, James P.. And the article was included in Journal of the American Chemical Society in 2014.Recommanded Product: 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

The catalytic enantioselective diboration of vinyl boronate esters furnishes chiral tris(boronates) in a selective fashion. Subsequent deborylative alkylation occurs in a diastereoselective fashion, both for intermol. and intramol. processes. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Recommanded Product: 1-Bromo-6-chlorohexane).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 1-Bromo-6-chlorohexane

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

New ω-chloroalkyl-substituted isatins and isoindigo was written by Bogdanov, A. V.;Kuz’micheva, T. A.;Mironov, V. F.. And the article was included in Russian Journal of Organic Chemistry in 2017.Formula: C6H12BrCl The following contents are mentioned in the article:

New 1-(ω-chloroalkyl)isatins were synthesized by alkylation of isatin with α-bromo-ω-chloroalkanes. Deoxygenation of 1-(3-chloropropyl)isatin with tris(diethylamino)phosphine results in selective formation of an isoindigo derivative This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Formula: C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.Formula: C6H12BrCl

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

Highly Regio- and Stereoselective Synthesis of Multialkylated Olefins through Carbozirconation of Alkynylboronates and Sequential Negishi and Suzuki-Miyaura Coupling Reactions was written by Nishihara, Yasushi;Okada, Yoshiaki;Jiao, Jiao;Suetsugu, Masato;Lan, Ming-Tzu;Kinoshita, Megumi;Iwasaki, Masayuki;Takagi, Kentaro. And the article was included in Angewandte Chemie, International Edition in 2011.Computed Properties of C6H12BrCl The following contents are mentioned in the article:

Regioselective and stereoselective synthesis of multialkylated olefins, e.g. I, via carbozirconation of alkynylboronates and sequential Negish and Suzuki-Miyaura coupling reaction was reported. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Computed Properties of C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Computed Properties of C6H12BrCl

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

Heat Capacity of α,ω-Bromochloroalkanes and α,ω-Dibromoalkanes: Their Dependence on the Hydrocarbon Chain Length and Temperature (285.15 to 355.15) K [Erratum to document cited in CA156:296087] was written by Goralski, Pawel;Tkaczyk, Mariola. And the article was included in Journal of Chemical & Engineering Data in 2012.Recommanded Product: 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

On page 793, Table 4 and Figure 2 contained errors in the C_p data; the corrected table and figure are given. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Recommanded Product: 1-Bromo-6-chlorohexane).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides can cause corrosion in pipelines, valves and condensers, and cause catalyst poisoning. The hydrocarbon processing industry (HPI) and others are affected by damage caused by these substances. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Recommanded Product: 1-Bromo-6-chlorohexane

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

Synthesis of acyclic alkanes by metal substitution with extension of the carbon framework was written by Kantchev, E. A. B.;Organ, M. G.. And the article was included in Science of Synthesis in 2009.COA of Formula: C6H12BrCl The following contents are mentioned in the article:

A review of methods to prepare acyclic alkanes by metal substitution with extension of the carbon framework. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3COA of Formula: C6H12BrCl).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Organochlorine compounds are lipophylic, meaning they are more soluble in fat than in water. This gives them a high tenancy to accumulate in the food chain (biomagnification).COA of Formula: C6H12BrCl

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

Evaluating the synthesis of bis-pyrazolines was written by Mahmoodi, Nosrat O.;Sharifzadeh, Bahman;Mamaghani, Manouchehr;Tabatabaeian, Khalil. And the article was included in Journal of Heterocyclic Chemistry in 2014.Recommanded Product: 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

The bis-cyclization of chalcone with thiosemicarbazide under basic condition led to the formation of thiocarbamoyl bis-pyrazolines. Bis-chalcones were prepared by a Claisen-Schmidt condensation between 1 mol dialdehyde and 2 mol acetophenones in the presence of NaOH as a catalyst. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Recommanded Product: 1-Bromo-6-chlorohexane).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. Aryl chlorides may be prepared by the Friedel-Crafts halogenation, using chlorine and a Lewis acid catalyst.Recommanded Product: 1-Bromo-6-chlorohexane

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

A three-photon probe with dual emission colors for imaging of Zn(II) ions in living cells was written by Mandal, Amal Kumar;He, Tingchao;Maji, Swarup Kumar;Sun, Handong;Zhao, Yanli. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2014.Name: 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

A novel three-photon probe for the imaging of exogenous Zn(II) ions in live cells with varying emission colors under three-photon excitation is developed. The tuning of the charge transfer state and the emission color of the probe was also demonstrated in the presence of acid. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Name: 1-Bromo-6-chlorohexane).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Organochlorines are organic compounds having multiple chlorine atoms. They were the first synthetic pesticides that were used in agriculture. They are resistant to most microbial and chemical degradations. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.Name: 1-Bromo-6-chlorohexane

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

Differentiating C-Br and C-Cl Bond Activation by Using Solvent Polarity: Applications to Orthogonal Alkyl-Alkyl Negishi Reactions was written by Hadei, Niloufar;Achonduh, George T.;Valente, Cory;O’Brien, Christopher J.;Organ, Michael G.. And the article was included in Angewandte Chemie, International Edition in 2011.SDS of cas: 6294-17-3 The following contents are mentioned in the article:

Orthogonal reactivity of bifunctional or unactivated bromochloroalkanes was observed in a double Negishi alkyl-alkyl cross-coupling reaction. This was made possible by a relatively simple solvent polarity trigger, lending itself to a one-pot approach. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3SDS of cas: 6294-17-3).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. Chlorination modifies the physical properties of hydrocarbons in several ways. These compounds are typically denser than water due to the higher atomic weight of chlorine versus hydrogen. The haloform reaction, using chlorine and sodium hydroxide, is also able to generate alkyl halides from methyl ketones, and related compounds. Chloroform was formerly produced thus.SDS of cas: 6294-17-3

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

Preparation of 2-(2-((6-chlorohexyl)oxy)ethoxy)ethanamine was written by Liu, Run-feng;Zhang, Heng;Zhong, Wu. And the article was included in Huaxue Shiji in 2011.Product Details of 6294-17-3 The following contents are mentioned in the article:

A new method for the preparation of 2-(2-((6-chlorohexyl)oxy)ethoxy)ethanamine is described. 2-(2-Aminoethoxy)ethanol was protected by BOC group, followed by etherification and deprotection, providing the titled compd in overall yield of 11.4%. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Product Details of 6294-17-3).

1-Bromo-6-chlorohexane (cas: 6294-17-3) belongs to organic chlorides. An organic chloride is an organic compound containing at least one covalently bonded atom of chlorine. Their wide structural variety and divergent chemical properties lead to a broad range of names and applications. Alkyl chlorides readily react with amines to give substituted amines. Alkyl chlorides are substituted by softer halides such as the iodide in the Finkelstein reaction.Product Details of 6294-17-3

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