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Merck
CN

432229

4-溴-2-氯-1-氟苯

99%

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关于此项目

线性分子式:
BrC6H3(Cl)F
化学文摘社编号:
分子量:
209.44
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
405-580-2
MDL number:
Assay:
99%
Form:
liquid
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assay

99%

form

liquid

refractive index

n20/D 1.553 (lit.)

bp

194 °C (lit.)

density

1.727 g/mL at 25 °C (lit.)

SMILES string

Fc1ccc(Br)cc1Cl

InChI

1S/C6H3BrClF/c7-4-1-2-6(9)5(8)3-4/h1-3H

InChI key

CJTIWGBQCVYTQE-UHFFFAOYSA-N

Application

4-Bromo-2-chloro-1-fluorobenzene may be used for the preparation of 2-(3-chloro-4-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane.


pictograms

Exclamation markEnvironment

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

192.2 °F - closed cup

flash_point_c

89 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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Mark S Jensen et al.
The Journal of organic chemistry, 70(15), 6034-6039 (2005-07-16)
A practical synthesis of 2-[3-(4-fluoro-3-pyridin-3-yl-phenyl)-imidazo[1,2-a]pyrimidin-7-yl]-propan-2-ol (1), an oral GABA(A) alpha(2/3)-selective agonist, is described. The five-step process, which afforded 1 in 40% overall yield, included imidazopyrimidine 2 and pyridine boronic acid 4 as key fragments. The synthesis is highlighted by consecutive
James A Newby et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 20(1), 263-271 (2013-12-18)
Conducting low-temperature organometallic reactions under continuous flow conditions offers the potential to more accurately control exotherms and thus provide more reproducible and scalable processes. Herein, progress towards this goal with regards to the lithium-halogen exchange/borylation reaction is reported. In addition



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货号GTIN
432229-10G04061837073519