Key Documents

View All Documentation

432229

4-Bromo-2-chloro-1-fluorobenzene

Name: 4-Bromo-2-chloro-1-fluorobenzene
Brand: ALDRICH

99%

Select a Size

Change View

About This Item

Linear Formula:

BrC₆H₃(Cl)F

CAS Number:

60811-21-4

Molecular Weight:

209.44

NACRES:

NA.22

PubChem Substance ID:

24867080

UNSPSC Code:

12352100

EC Number:

405-580-2

MDL number:

MFCD00051794

Assay:

99%

Form:

liquid

Technical Service

Need help? Our team of experienced scientists is here for you.

Let Us Assist

Properties

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

Description

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

GHS07,GHS09

signalword

Warning

hcodes

H302,H315,H410

pcodes

P264 - P273 - P280 - P301 + P312 - P302 + P352 - P332 + P313

Hazard Classifications

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

Storage Class

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

Regulatory Information

新产品

This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Efficient synthesis of a GABA A alpha2,3-selective allosteric modulator via a sequential Pd-catalyzed cross-coupling approach.

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

Investigation of a lithium-halogen exchange flow process for the preparation of boronates by using a cryo-flow reactor.

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

Global Trade Item Number

SKU	GTIN
432229-10G	04061837073519