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Merck

432229

Sigma-Aldrich

4-溴-2-氯-1-氟苯

99%

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About This Item

线性分子式:
BrC6H3(Cl)F
CAS号:
分子量:
209.44
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

化驗

99%

形狀

liquid

折射率

n20/D 1.553 (lit.)

bp

194 °C (lit.)

密度

1.727 g/mL at 25 °C (lit.)

SMILES 字串

Fc1ccc(Br)cc1Cl

InChI

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

InChI 密鑰

CJTIWGBQCVYTQE-UHFFFAOYSA-N

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應用

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.[1]

象形圖

Exclamation markEnvironment

訊號詞

Warning

危險聲明

危險分類

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

儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

WGK 3

閃點(°F)

192.2 °F - closed cup

閃點(°C)

89 °C - closed cup

個人防護裝備

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


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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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