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Bromobenzyl Chloride

Bromobenzyl Chloride Suppliers list
Company Name: SynQuest Laboratories, Inc.  
Tel: 904 462 0788
Email: info@synquestlabs.com
Products Intro: Cas:823-78-9
ProductName:3-Bromobenzyl bromide
Brand: SynQuest Laboratories | Product Number: 1700-9-W0
Company Name: Apollo Scientific Ltd  
Tel: 44-161-4060505
Email: ales@apo
Products Intro: Cas:823-78-9
ProductName:3-Bromobenzyl bromide
Company Name: Jinan Carbotang Biotech Co.,Ltd.
Tel: +8615866703830
Email: figo.gao@foxmail.com
Products Intro: Cas:823-78-9
ProductName:3-Bromobenzyl bromide
Purity: 98% | Package: 5KG;1KG
Company Name: Auonsi (Shanghai) Biology Technology Co., Ltd.  
Tel: 400-1107768 15058188853
Email: 478133536@qq.com
Products Intro: Cas:823-78-9
ProductName:3-Bromobenzyl bromide
Purity: 98% | Package: 5g;25g
Company Name:   
Tel:
Email: info@chaturyabiotech.com
Products Intro: Cas:823-78-9
ProductName:3-Bromobenzyl bromide
Purity: 99% | Package: 1 kg,5 kg, 10 kg,25kg and 1 MT

Bromobenzyl Chloride manufacturers

  • 2-BROMOBENZYL CHLORIDE
  • 2-BROMOBENZYL CHLORIDE pictures
  • $1.00
  • 2020-01-10
  • CAS:578-51-8
  • Min. Order: 1KG
  • Purity: 98% HPLC
  • Supply Ability: 10 tons/month
Bromobenzyl Chloride Basic information
Product Name:Bromobenzyl Chloride
Synonyms:3-Brombenzyl bromide;ALPHA,3-DIBROMOTOLUENE;ALPHA,M-DIBROMOTOLUENE;3-BROMOBENZYL BROMIDE;3-Bromo Benzyl Bromide m-Bromobenzyl Bromide;3-BromobenzylBromide98%;3-Bromobenzylbromide,99%;m-Bromobenzyl
CAS:823-78-9
MF:C7H6Br2
MW:249.93
EINECS:212-519-1
Product Categories:alkyl bromide;Aromatic Halides (substituted);bc0001;Benzyl
Mol File:823-78-9.mol
Bromobenzyl Chloride Structure
Bromobenzyl Chloride Chemical Properties
Melting point 39-41 °C(lit.)
Boiling point 130 °C12 mm Hg
density 1,56 g/cm3
refractive index 1.6066 (estimate)
Fp >230 °F
storage temp. Keep in dark place,Inert atmosphere,2-8°C
solubility Chloroform (Sparingly), Methanol (Slightly)
form Adhering Crystals or Crystalline Powder
color White
Water Solubility Insoluble in water.
BRN 2078683
InChIInChI=1S/C7H6Br2/c8-5-6-2-1-3-7(9)4-6/h1-4H,5H2
InChIKeyZPCJPJQUVRIILS-UHFFFAOYSA-N
SMILESC1(Br)=CC=CC(CBr)=C1
CAS DataBase Reference823-78-9(CAS DataBase Reference)
EPA Substance Registry SystemBenzene, 1-bromo-3-(bromomethyl)- (823-78-9)
Safety Information
Hazard Codes C
Risk Statements 34-37
Safety Statements 26-36/37/39-45-25
RIDADR UN 3261 8/PG 2
WGK Germany 3
F 19
TSCA TSCA listed
HazardClass 8
PackingGroup III
HS Code 29036990
Storage Class8A - Combustible corrosive hazardous materials
Hazard ClassificationsSkin Corr. 1B
MSDS Information
ProviderLanguage
3-Bromobenzyl bromide English
ACROS English
SigmaAldrich English
ALFA English
Bromobenzyl Chloride Usage And Synthesis
Chemical PropertiesWhite to yellow solid
Uses3-Bromobenzyl bromide was used in the synthesis of, 1,7-di(3-bromobenzyl)cyclen and substituted 8-arylquinoline, phosphodiesterase 4 (PDE4) inhibitors.
Uses3-Bromobenzyl bromide was used in the synthesis of:
  • 1,7-di(3-bromobenzyl)cyclen
  • substituted 8-arylquinoline, phosphodiesterase 4 (PDE4) inhibitors
General Description3-Bromobenzyl bromide undergoes reduction with diethylzinc in the presence of Pd(PPh3)4 to yield corresponding hydrocarbon.
Synthesis
3-Bromotoluene

591-17-3

3-Bromobenzyl bromide

823-78-9

General procedure for the synthesis of 3-bromobenzyl bromide from 3-bromomethylbenzene: To a mixture of N-bromosuccinimide (NXS) and substrate (1 or 6) in acetonitrile (CH3CN), silicon tetrachloride (SiCl4) was slowly added at room temperature, and the reaction mixture was stirred continuously until thin-layer chromatography (TLC) monitoring showed complete disappearance of the feedstock. Subsequently, the reaction mixture was poured into water and extracted with dichloromethane (CH2Cl2). All organic phase extracts were combined and dried with anhydrous magnesium sulfate (MgSO4), followed by concentration under reduced pressure to remove the solvent. The residue was purified by recrystallization (petroleum ether-ether, 3:1) to give the pure products 2b-2g or 3b; or by silica gel column chromatography (hexane-ethyl acetate, 10:1 or 30:1) to give the pure products 2a, h, i, 3a-5 or 7-9.

References[1] Journal of Organic Chemistry, 2014, vol. 79, # 1, p. 223 - 229
[2] Synthetic Communications, 2010, vol. 40, # 7, p. 998 - 1003
[3] Tetrahedron Letters, 2011, vol. 52, # 31, p. 4026 - 4029
[4] Patent: US2009/12171, 2009, A1. Location in patent: Page/Page column 11
[5] Patent: WO2005/105736, 2005, A1. Location in patent: Page/Page column 28
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