28598-82-5

Basic information

• Product Name: 1-chloro-8-bromooctane
• Synonyms: Octane, 1-bromo-8-chloro-; 1-Bromo-8-chlorooctane
• CAS NO: 28598-82-5
• Molecular Formula: C₈H₁₆BrCl
• Molecular Weight: 227.5720
• Mol File: 28598-82-5.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: 1-chloro-8-bromooctane(CAS DataBase Reference)
• NIST Chemistry Reference: 1-chloro-8-bromooctane(28598-82-5)
• EPA Substance Registry System: 1-chloro-8-bromooctane(28598-82-5)

Safety Data

• Hazardous Substances Data: 28598-82-5(Hazardous Substances Data)

Usage

General Description

1-Chloro-8-bromooctane is a chemical compound that belongs to the class of organic compounds known as halohydrocarbons. This specific chemical compound has chlorine and bromine as halogens. The key feature in its structure is an eight-carbon chain with a chlorine atom attached to the first carbon and a bromine atom attached to the eighth carbon. Widely used in organic synthesis, the primary use of 1-Chloro-8-bromooctane is as a reactant to create other chemicals, due to its versatile properties and its ability to participate in various types of chemical reactions. The toxicity and environmental impact of this compound can vary based on the extent and nature of exposure.

Upstream product

• 593-14-6 1-chloro-8-fluorooctane 
• 123455-82-3 Pyridine-2-sulfonic acid 8-chloro-octyl ester 
• 23144-52-7 8-chlorooctan-1-ol 
• 50816-19-8 8-bromooctanol 

Downstream Products

• 1616593-45-3 3,6-dimethyl-1,2-di(8-chlorooctoxy)benzene 
• 1616593-38-4 3,6-dimethyl-4,5-di(8-chlorooctoxy)-1,2-diisocyanobenzene 
• 1642301-69-6 C₂₆H₄₂Cl₂N₂O₄ 
• 1616593-44-2 3,6-dimethyl-1,2-di(8-chlorooctoxy)benzene 
• 131802-03-4 C₈H₁₆Cl₄Si 
• 173446-84-9 ethyl [8(Z),11(Z),14-pentadecatrienyl]salicylate 
• 332011-49-1 ethyl [8(Z),11(Z)-pentadecadienyl]salicylate 
• 332011-45-7 ethyl 6-(8-iodooctyl)-2-methoxybenzoate 
• 332011-43-5 ethyl 6-(8-chlorooctyl)salicylate 
• 332011-44-6 ethyl 6-(8-chlorooctyl)-2-methoxybenzoate 
• 217449-17-7 ethyl 6-<8(Z)-pentadecenyl>salicylate 
• 332011-48-0 ethyl 2-methoxy-6-[8(Z),11(Z),14-pentadecatrienyl]benzoate 
• 188579-53-5 ethyl 2-methoxy-6-[8(Z),11(Z)-pentadecadienyl]benzoate 
• 114802-12-9 ethyl 2-methoxy-6-[8(Z)-pentadecenyl]benzoate 

Relevant articles and documents

Halogen Exchange Reaction of Aliphatic Fluorine Compounds with Organic Halides as Halogen Source

The halogen exchange reaction of aliphatic fluorine compounds with organic halides as the halogen source was achieved. Treatment of alkyl fluorides (primary, secondary, or tertiary fluorides) with a catalytic amount of titanocene dihalides, trialkyl aluminum, and polyhalomethanes (chloro or bromo methanes) as the halogen source gave the corresponding alkyl halides in excellent yields under mild conditions. In the case of a fluorine/iodine exchange, no titanocene catalyst is needed. Only C-F bonds are selectively activated under these conditions, whereas alkyl chlorides, bromides, and iodides are tolerant to these reactions.

Lengthening alkyl spacers to increase SBA-15-anchored Rh-P complex activities in 1-octene hydroformylation

The alkyl spacer was lengthened in heterogenizing a Rh-P complex into mesoporous silicate SBA-15 to increase the immobilized catalyst activities in 1-octene hydroformylation. The Royal Society of Chemistry.

Room-temperature alkyl-alkyl Suzuki cross-coupling of alkyl bromides that possess β hydrogens [1]

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