75534-18-8

Basic information

• Product Name: Benzene, 1-bromo-2-(2-chloroethyl)-
• CAS NO: 75534-18-8
• Molecular Formula: C8H8BrCl
• Molecular Weight: 219.509
• Mol File: 75534-18-8.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1-bromo-2-(2-chloroethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-bromo-2-(2-chloroethyl)-(75534-18-8)
• EPA Substance Registry System: Benzene, 1-bromo-2-(2-chloroethyl)-(75534-18-8)

Safety Data

• Hazardous Substances Data: 75534-18-8(Hazardous Substances Data)

Upstream product

• 6630-33-7 ortho-bromobenzaldehyde 
• 130089-19-9 1-bromo-2-(2-methoxyethenyl)benzene 
• 96557-30-1 2-bromophenylacetaldehyde 
• 1074-16-4 2-bromophenylethyl alcohol 
• 103-82-2 phenylacetic acid 

Downstream Products

• 1379674-62-0 1-(2-chloroethyl)-2-ethynylbenzene 
• 1379674-99-3 C₁₃H₁₇ClSi 
• 2039-88-5 2-bromostyrene 
• 406954-89-0 1-[2-(2-bromophenyl)ethyl]-4-(cyclohexylcarbonyl)-1,3,4-trihydropyrazin-2-one 
• 31236-96-1 1-phenyl-2,3-dihydrobenzo[b]phosphole-1-oxide 
• 108954-95-6 1-phenyl-2,3-dihydro-1H-arsindole 
• 1238588-10-7 C₈H₁₀BClO₂ 
• 1033629-58-1 sodium 2-(2-bromo-phenyl)ethanesulfonate 
• 1961-97-3 3-phenyl-1H-indene 
• 30516-40-6 3-phenyl-2,3-dihydro-1H-inden-1-ol 
• 319493-66-8 5-[2-(2-chloroethyl)phenyl]dihydrofuran-2-one 

Relevant articles and documents

Synthesis and characterization of 1-methyl-1-silaindane and 1-methyl-1-germaindane

New synthetic routes to 1-methyl-1-silaindane (1b) and 1-methyl-1-germaindane (1b) were developed and the desired products were obtained in good isolated yield. Compounds 1a and 1b were fully characterized by mass spectroscopy, 1H and 13/

One-pot synthesis of aminoenone via direct reaction of the chloroalkyl enone with NaN3: Rapid access to polycyclic alkaloids

(Figure presented) A new one-pot procedure for the preparation of aminoenone from chloroalkyl enone and sodium azide was demonstrated. The structure of the presumed triazoline intermediate in this process was confirmed by X-ray analysis for the first time. As the application of this methodology, the synthesis of polycyclic alkaloid hexahydroapoerysopine (1a) was achieved through an efficient synthetic route.

Lithiophenylalkyllithiums: New dilithium reagents having both sp2- and sp3-hybridised remote carbanionic centres

The reaction of chloro-(2-chloroethyl)benzenes (1), 4-chloro-(3-chloropropyl)benzene (3) or 4-chlorophenyl chloromethyl ether (5) with lithium power using naphthalene as the electron shuttle (8 mol%) in the presence of different carbonyl compounds [Busub