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4-bromophenyl, also known as 1-bromo-4-phenyl, is an organic compound consisting of a bromo substituent attached to a phenyl ring. It is a colorless, crystalline solid with a molecular formula of C6H5Br. 4-bromophenyl is widely used in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals due to its reactivity and stability. 4-bromophenyl can be synthesized through electrophilic bromination of benzene or by the reaction of phenylmagnesium bromide with elemental bromine. It is an important building block in the chemical industry and plays a crucial role in the development of new compounds with potential applications in various fields.

2973-43-5

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2973-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2973-43-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 3 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2973-43:
(6*2)+(5*9)+(4*7)+(3*3)+(2*4)+(1*3)=105
105 % 10 = 5
So 2973-43-5 is a valid CAS Registry Number.

2973-43-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Bromophenyl

1.2 Other means of identification

Product number -
Other names 4-Brom-phenylradikal

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2973-43-5 SDS

2973-43-5Downstream Products

2973-43-5Relevant academic research and scientific papers

NONSELECTIVE DISPROPORTIONATION OF ISOMERIC HYDROXYCYCLOHEXADIENYL RADICALS TO PHENOLS

Tezuka, Takahiro,Marusawa, Hiroshi,Ichikawa, Kazuhiko

, p. 2145 - 2148 (2007/10/02)

Comparison of the isomer ratios and yields of cresol, methoxyphenol, and nitrophenol, which were obtained by the aromatic hydroxylation with hydroxyl radical in the presence or absence of benzoquinones in anhydrous media, indicates that disproportionation of hydroxycyclohexadienyl radicals occurs nonselectively.

Free-Radical Reductions of Arenediazonium Ions in Aqueous Solution. V. Pulse-Radiolytic Determination of Rate Constants for Some para-Substituted Benzenediazonium Ions

Packer, John E.,Moenig, Joerg,Dobson, Brian C.

, p. 1433 - 1441 (2007/10/02)

Some rate constants for the reduction of para-substituted benzenediazonium ions by the radicals eaq-, .CH2OH, (CH3)2.COH and some semiquinone radical anions have been measured.The substituent group has no effect on the rates with eaq-, but as the reduction potential of the reducing radical becomes more positive, the substituent effect increases, electron-withdrawing groups enhancing the rates.No free halide is formed on reduction of p-BrC6H4N2+ or p-IC6H4N2+ by eaq- or .CH2OH.

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