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α-Bromo-α-(4-methoxyphenyl)acetonitrile is an organic compound with the chemical formula C9H8BrNO. It is a derivative of acetonitrile, featuring a bromine atom attached to the alpha carbon and a 4-methoxyphenyl group on the same carbon. α-Bromo-α-(4-methoxyphenyl)acetonitrile is a colorless to pale yellow solid and is soluble in organic solvents. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of pesticides and other specialty chemicals. Due to its reactivity, it is important to handle α-Bromo-α-(4-methoxyphenyl)acetonitrile with care, following proper safety protocols.

58327-36-9

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58327-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 58327-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,3,2 and 7 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58327-36:
(7*5)+(6*8)+(5*3)+(4*2)+(3*7)+(2*3)+(1*6)=139
139 % 10 = 9
So 58327-36-9 is a valid CAS Registry Number.

58327-36-9SDS

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 α-Bromo-α-(4-methoxyphenyl)acetonitrile

1.2 Other means of identification

Product number -
Other names α-Brom-p-methoxybenzylcyanid

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:58327-36-9 SDS

58327-36-9Upstream product

58327-36-9Relevant academic research and scientific papers

Some derivatives of 2,4 diamino 5 phenylthiazole (amiphenazole)

Adams,Nicholls,Williams

, p. 425 - 427 (2007/10/05)

To facilitate metabolic studies on the analeptic 2,4 diamino 5 phenylthiazole (Amiphenazole) attempts were made to synthesise 2,4 diamino 5 (p hydroxyphenyl) thiazole (unsuccessful) and 2,4 dihydroxy 5 (p hydroxyphenyl) thiazole (successful) as possible metabolites. The pharmacology of some synthetic intermediates revealed that 2,4 diamino 5 (p methoxyphenyl) thiazole was a more potent stimulant than Amiphenazole in morphine depressed respiration of rabbits whilst therapeutic indices were comparable. 2,4 Diamino 5 (p benzyloxyphenyl) thiazole depressed locomotor activity in mice. 2,4 Dihydroxy 5 (p hydroxyphenyl) thiazole did not affect morphine induced analgesia in mice.

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