5-Chloro-2-fluorobenzyl bromide
5-Chloro-2-fluorobenzyl bromide Basic information
- Product Name:
- 5-Chloro-2-fluorobenzyl bromide
- Synonyms:
-
- 5-CHLORO-2-FLUOROBENZYL BROMIDE
- alpha-Bromo-3-chloro-6-fluorotoluene
- à-bromo-3-chloro-6-fluorotoluene
- 5-Chloro-2-fluoronitrobenzenebenzyl bromide
- 2-Fluoro-5-chlorobenzyl bromide
- 2-(Bromomethyl)-4-chloro-1-fluorobenzene
- 1-(Bromomethyl)-5-chloro-2-fluorobenzene
- -bromo-3-chloro-6-fluorotoluene
- CAS:
- 71916-91-1
- MF:
- C7H5BrClF
- MW:
- 223.47
- EINECS:
- 670-703-0
- Product Categories:
-
- Fluorine series
- Mol File:
- 71916-91-1.mol
5-Chloro-2-fluorobenzyl bromide Chemical Properties
- Melting point:
- 45°/0.5mm
- Boiling point:
- 44-45°C 0,5mm
- Density
- 1.65
- refractive index
- 1.565
- Flash point:
- 44-45°C/0.5mm
- storage temp.
- under inert gas (nitrogen or Argon) at 2-8°C
- form
- clear liquid
- color
- Colorless to Light yellow to Light orange
- Sensitive
- Lachrymatory
- BRN
- 637765
- CAS DataBase Reference
- 71916-91-1(CAS DataBase Reference)
Safety Information
- Hazard Codes
- C,Xn
- Risk Statements
- 34-36/37/38-22
- Safety Statements
- 26-36/37/39-45
- RIDADR
- 3265
- Hazard Note
- Corrosive/Lachrymatory
- HazardClass
- 8
- PackingGroup
- III
- HS Code
- 29039990
MSDS
- Language:English Provider:5-Chloro-2-fluorobenzyl bromide
- Language:English Provider:ALFA
5-Chloro-2-fluorobenzyl bromide Usage And Synthesis
Uses
2-(bromomethyl)-4-chloro-1-fluoro-Benzene is a useful reactant which has been used in the synthesis of potential cell cycle inhibitors in HepG2 cells.
Synthesis
452-66-4
71916-91-1
General procedure for the synthesis of 5-chloro-2-fluorobenzyl bromide from 5-chloro-2-fluorotoluene: A: 5-Chloro-2-fluorotoluene (100 g, 692 mmol) was dissolved in ethyl acetate (300 ml) at 20 °C. To this solution N-bromosuccinimide (147.7 g, 830 mmol) and dibenzoyl peroxide (2 g, 8.25 mmol) were added sequentially. The reaction mixture was heated to 80 °C and stirred for 3 hours. Upon completion of the reaction, heptane (300 ml) was added and the mixture was cooled to 0 °C, at which time the succinimide precipitated. After filtration and washing with heptane, the residue was washed with water (1500 ml). The filtrate was concentrated to dryness under vacuum to give 162 g of the crude product 5-chloro-2-fluorobenzyl bromide. The crude product (141 g) was purified by vacuum distillation at 99 °C and 33 mbar to give the final 5-chloro-2-fluorobenzyl bromide (99 g, 75% yield). The purity of the product was analyzed by GC to be 87.1% (% area).1H-NMR (CDCl3) data: δ 4.44 (2H, d, CH2), 7.01 (1H, t, H3), 7.26 (1H, m, H4), 7.38 (1H, m, H6).
References
[1] Journal of Heterocyclic Chemistry, 1997, vol. 34, # 1, p. 27 - 32
[2] Patent: WO2008/3460, 2008, A1. Location in patent: Page/Page column 23-24
[3] Patent: US2008/9619, 2008, A1. Location in patent: Page/Page column 11-12
[4] Journal of Medicinal Chemistry, 1991, vol. 34, # 10, p. 3098 - 3105
[5] Journal of the Chemical Society - Perkin Transactions 1, 1997, # 19, p. 2903 - 2909
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5-Chloro-2-fluorobenzyl bromide(71916-91-1)Related Product Information
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- Benzyl chloroformate
- Chlorobromoisocyanurate
- 1-Bromo-3-chloro-5,5-dimethylhydantoin
- 1,2-Difluorobenzene
- Ethidium bromide
- Sodium bromate
- 2-Chlorobenzyl chloride
- BRETYLIUM TOSYLATE
- alpha-Chloro-o-fluorotoluene
- Transfluthrin
- Florfenicol
- 4-Fluorobenzaldehyde
- 4-Fluorobenzyl chloride
- Difluorochloromethane
- Methyl bromide
- FENFLURAMINE
- 3-CHLORO-2,6-DIFLUOROBENZYL BROMIDE