40422-70-6

Basic information

• Product Name: 3-BROMOPHENETHYL BROMIDE 97
• Synonyms: 3-BROMOPHENETHYL BROMIDE 97;1-broMo-3-(2-broMoethyl)benzene;3-BroMophenethyl broMide 97%;1-Bromo-3-(2-bromoethyl)
• CAS NO: 40422-70-6
• Molecular Formula: C₈H₈Br₂
• Molecular Weight: 263.959
• Mol File: 40422-70-6.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 77-78 °C0.1 mm Hg
• Flash Point: >230 °F
• Appearance: /
• Density: 1.725 g/mL at 25 °C
• Vapor Pressure: 0.0128mmHg at 25°C
• Refractive Index: n20/D 1.595
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 3-BROMOPHENETHYL BROMIDE 97(CAS DataBase Reference)
• NIST Chemistry Reference: 3-BROMOPHENETHYL BROMIDE 97(40422-70-6)
• EPA Substance Registry System: 3-BROMOPHENETHYL BROMIDE 97(40422-70-6)

Safety Data

• Hazard Codes: Xn,N
• Statements: 22-43-51/53
• Safety Statements: 36/37-61
• RIDADR: UN 3082 9 / PGIII
• WGK Germany: 2
• Hazardous Substances Data: 40422-70-6(Hazardous Substances Data)

Usage

General Description

3-Bromophenethyl bromide 97 is a chemical compound with the molecular formula C8H8Br2. It is a brominated benzene derivative that is commonly used in organic synthesis and as a reagent in the preparation of various organic compounds. 3-BROMOPHENETHYL BROMIDE 97 exists as a colorless to pale yellow liquid with a boiling point of 232-234°C. It is primarily used as a chemical intermediate in the production of pharmaceuticals, agrochemicals, and other organic products. 3-Bromophenethyl bromide 97 is a highly reactive and potentially hazardous substance that should be handled with caution and in accordance with all relevant safety protocols.

InChI:InChI=1/C8H8Br2/c9-5-4-7-2-1-3-8(10)6-7/h1-3,6H,4-5H2

Upstream product

• 75-25-2 Bromoform 
• 765-46-8 spiro[2.4]hepta-4,6-diene 
• 64723-45-1 toluene-4-sulfonic acid-(3-bromo-phenethyl ester) 
• 28229-69-8 2-(3-bromophenyl)ethan-1-ol 
• 1878-67-7 3-Bromophenylacetic acid 
• 2039-86-3 3-bromostyrene 

Downstream Products

• 57186-65-9 1-bromo-3-(2'-iodoethyl)benzene 
• 2039-86-3 3-bromostyrene 
• 1000885-75-5 (1-(3-bromophenethyl)piperidin-4-yl)(4-fluorophenyl)methanone 
• 439856-34-5 (1-(3-iodophenethyl)piperidin-4-yl)(4-fluorophenyl)methanone 
• 1020264-96-3 5,7-dibromo-1-[2-(3-bromophenyl)ethyl]-1H-indole-2,3-dione 
• 1202932-45-3 4-Bromo-2-(2-bromo-ethyl)-benzenesulfonyl chloride 
• 1352576-03-4 Br^(1-)*C₂₉H₃₈BrN₂O₂⁽¹⁺⁾ 
• 1382354-32-6 2-{3-(3-bromophenethoxy)phenylamino}benzamide 
• 785032-26-0 2-(3-bromophenyl)-N-methylethanamine 
• 1415676-45-7 C₁₆H₁₇BrN₄O₂S 
• 1449689-91-1 1-bromo-3-(4-(4-methoxyphenyl)but-3-yn-1-yl)benzene 
• 172484-94-5 (1S,2R)-4-Bromo-3-(2-bromo-ethyl)-cyclohexa-3,5-diene-1,2-diol 
• 1225280-80-7 1-(3-bromophenethyl)pyrrolidine 
• 1613028-81-1 N-(3-bromophenethyl)-2,4,6-trimethyl-N-((3'-(methylsulfonyl)-[1,1'-biphenyl]-4-yl)methyl)benzenesulfonamide 

Relevant articles and documents

Cascade bio-hydroxylation and dehalogenation for one-pot enantioselective synthesis of optically active β-halohydrins from halohydrocarbons

A stereoselective hydroxylation and enantioselective dehalogenation cascade reaction was developed for the synthesis of optically active β-haloalcohols from halohydrocarbons. This cascade system employed P450 and halohydrin dehalogenase as two compatible biocatalysts, allowing a straightforward, greener and efficient access to β-halohydrins with excellent enantioselectivities (98-99%).

Synthesis and in vivo evaluation in mice of (123I)-(4- fluorophenyl)(1-(3-iodophenethyl)piperidin-4-yl) methanone as a potential SPECT-tracer for the serotonin 5-HT2A receptor

This work reports the synthesis, radiolabelling and in vivo evaluation in NMRI mice of [123I]-(4-fluorophenyl)[1-(3-iodophenethyl)piperidin-4- yl]methanone ([123I]-3-I-CO) as a potential SPECT tracer for the 5-HT2A recepto

REACTIONS OF DIHALOCARBENES WITH SUBSTITUTED SPIROHEPTA-4,6-DIENES

Reactions of dihalocarbenes with spirohepta-4,6-diene lead to the formation of 1-halo-3-(2-haloethyl)benzenes, which readily undergo dehydrohalogenation to 3-halostyrenes.From 1-arylspirohepta-4,6-dienes and dihalocarbenes 3-halostilbenes are obtained.