Category: 6294-17-3

Organophoto-redox-Catalyzed Formation of Alkyl-Aryl and -Alkyl C-S/Se Bonds from Coupling of Redox-Active Esters with Thio/Selenosulfonates was written by Dong, Yue;Ji, Peng;Zhang, Yueteng;Wang, Changqing;Meng, Xiang;Wang, Wei. And the article was included in Organic Letters in 2020.HPLC of Formula: 6294-17-3 The following contents are mentioned in the article:

A mild organophoto-redox synthetic protocol for forming a C_sp³-S/Se bond by reacting widespread redox-active esters with thio/selenosulfonates has been developed. The power of the synthetic manifold is fueled by an unprecedented broad substrate scope and wide functional group tolerance. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3HPLC of Formula: 6294-17-3).

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.While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available. Alkyl chlorides readily undergo attack by nucleophiles.HPLC of Formula: 6294-17-3

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

Ni-Catalyzed Carboxylation of Unactivated Alkyl Chlorides with CO₂ was written by Borjesson, Marino;Moragas, Toni;Martin, Ruben. And the article was included in Journal of the American Chemical Society in 2016.Computed Properties of C6H12BrCl The following contents are mentioned in the article:

A catalytic carboxylation of unactivated primary, secondary, and tertiary alkyl chlorides with CO₂ at atm. pressure is described. This protocol represents the first intermol. cross-electrophile coupling of unactivated alkyl chlorides, thus leading to new knowledge in the cross-coupling arena. 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. 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.Computed Properties of C6H12BrCl

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

Dual Catalytic Platform for Enabling sp³ α C-H Arylation and Alkylation of Benzamides was written by Rand, Alexander W.;Yin, Hongfei;Xu, Liang;Giacoboni, Jessica;Martin-Montero, Raul;Romano, Ciro;Montgomery, John;Martin, Ruben. And the article was included in ACS Catalysis in 2020.Safety of 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

A dual catalytic sp³ α C-H arylation and alkylation of benzamides with organic halides is described. This protocol exhibits an exquisite site selectivity, chemoselectivity, and enantioselectivity pattern, offering a complementary reactivity mode to existing sp³ arylation or alkylations via transition metal catalysis or photoredox events. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Safety of 1-Bromo-6-chlorohexane).

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. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Safety of 1-Bromo-6-chlorohexane

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

C-C Bond Formation via Copper-Catalyzed Conjugate Addition Reactions to Enones in Water at Room Temperature was written by Lipshutz, Bruce H.;Huang, Shenlin;Leong, Wendy Wen Yi;Isley, Nicholas A.. And the article was included in Journal of the American Chemical Society in 2012.Category: chlorides-buliding-blocks The following contents are mentioned in the article:

Conjugate addition reactions to enones can now be done in water at room temperature with in situ generated organocopper reagents. Mixing an enone, zinc powder, TMEDA, and an alkyl halide in a micellar environment containing catalytic amounts of Cu(I), Ag(I), and Au(III) leads to 1,4-adducts in good isolated yields: no organometallic precursor need be formed. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Category: chlorides-buliding-blocks).

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. 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).Category: chlorides-buliding-blocks

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

Palladium-Catalyzed Hydroalkylation of Styrenes with Organozinc Reagents To Form Carbon-Carbon sp³-sp³ Bonds under Oxidative Conditions was written by Urkalan, Kaveri Balan;Sigman, Matthew S.. And the article was included in Journal of the American Chemical Society in 2009.Formula: C6H12BrCl The following contents are mentioned in the article:

An unconventional route for the formation of sp³-sp³ C-C bonds from various styrenes and an organozinc reagent in a formal alkene hydroalkylation process is detailed. Mechanistically, this process is proposed to proceed by initial transmetalation followed by formation of a Pd-H species, which is subsequently trapped by the styrene. 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. Organic chlorides are compounds containing a carbon-chlorine bond, which are widely used in the oil field as a wax dissolver. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Formula: C6H12BrCl

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

Synthesis of novel analogs 3,4-dihydro-1H-quinolin-2-one derivatives as typical Antidepressant, Sedative and anti-Parkinson agents was written by Pai, Nandini R.;Pusalkar, Deeptaunshu Atul;Khandekar, Dileep. And the article was included in Heterocyclic Letters in 2012.COA of Formula: C6H12BrCl The following contents are mentioned in the article:

This study aimed at synthesis of the potential Antidepressant and Sedative, anti-Parkinson’s activity of structurally diverse derivatives of lead compound 3,4-dihydro-1H-quinolin-2-one; synthesized via straightforward and efficient synthetic process. The structures of the compounds were characterized by spectral data (IR and 1H-NMR). 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. Organic chlorides can be used in production of: PVC, pesticides, chloromethane, teflon, insulators. 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

Bis(phenylsulfonyl)methane mediated synthesis of olefins via a halogen elimination and double bond migration was written by Jiang, Jing;Hu, Ying;Cai, Xin;Wang, Liudi;Hu, Yanwei;Chen, Shaohua;Zhang, Shilei;Zhang, Yinan. And the article was included in Organic & Biomolecular Chemistry in 2018.Safety of 1-Bromo-6-chlorohexane The following contents are mentioned in the article:

An effective dehydrochlorination of bis(phenylsulfonyl)alkanes to prepare alkene building blocks was developed. The elimination together with double bond migration resulted in a variety of β,γ-unsaturated bis(phenylsulfonyl)olefins in good yields with only E geometry. The following chem. diversification represented an easy and straightforward access to a series of alkene building blocks. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Safety of 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. 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.Safety of 1-Bromo-6-chlorohexane

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

Nickel-Catalyzed Reductive Amidation of Unactivated Alkyl Bromides was written by Serrano, Eloisa;Martin, Ruben. And the article was included in Angewandte Chemie, International Edition in 2016.Recommanded Product: 6294-17-3 The following contents are mentioned in the article:

A user-friendly, nickel-catalyzed reductive amidation of unactivated primary, secondary, and tertiary alkyl bromides with isocyanates is described. This catalytic strategy offers an efficient synthesis of a wide range of aliphatic amides under mild conditions and with an excellent chemoselectivity profile while avoiding the use of stoichiometric and sensitive organometallic reagents. This study involved multiple reactions and reactants, such as 1-Bromo-6-chlorohexane (cas: 6294-17-3Recommanded Product: 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. Aliphatic organochlorides are often alkylating agents as chlorine can act as a leaving group, which can result in cellular damage.Recommanded Product: 6294-17-3

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

Preparation of highly functionalized alkylzinc halides from alkyl bromides using Mg, ZnCl₂ and LiCl was written by Bluemke, Tobias D.;Piller, Fabian M.;Knochel, Paul. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2010.COA of Formula: C6H12BrCl The following contents are mentioned in the article:

Alkyl bromides bearing various functional groups are smoothly converted to functionalized alkylzinc reagents by the direct insertion of magnesium in the presence of LiCl and ZnCl₂. These organozinc derivatives are used in situ for palladium-catalyzed cross-coupling reactions and additions to electrophiles such as aroyl chlorides, allyl bromides, and sulfonothioates. 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. 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. Alkanes and aryl alkanes may be chlorinated under free radical conditions, with UV light. However, the extent of chlorination is difficult to control.COA of Formula: C6H12BrCl

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

Methylene chain ruler for evaluating the regioselectivity of a substrate-recognizing oxidation catalyst was written by Teramae, Shota;Kito, Akane;Shingaki, Tomoteru;Hamaguchi, Yu;Yano, Yuuki;Nakayama, Takamori;Kobayashi, Yuko;Kato, Nobuki;Umezawa, Naoki;Hisamatsu, Yosuke;Nagano, Tetsuo;Higuchi, Tsunehiko. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2019.SDS of cas: 6294-17-3 The following contents are mentioned in the article:

Regioselective C-H oxidation of aliphatic mols. with synthetic catalysts is challenging. The authors incorporated substrate-recognition sites into a Ru porphyrin-heteroaromatic N-oxide catalytic system to characterize its regioselectivity for the oxidation of alkanes. This substrate-recognition catalytic reaction exhibits high regioselectivity and high reaction efficiency. 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. Organochlorines stimulate the central nervous system and cause convulsions, tremor, nausea, and mental confusion. Examples are dichlorodiphenyltrichloroethane (DDT), chlordane, lindane, endosulfan, and dieldrin. 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.SDS of cas: 6294-17-3

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