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2-Bromo-2-(m-tolyl)acetonitrile is an organic compound characterized by its molecular formula C9H8BrN. It is a derivative of acetonitrile, featuring a bromine atom and a meta-tolyl group (a methyl group attached to the meta position of a benzene ring). This chemical is a colorless to pale yellow liquid with a density of 1.42 g/cm3 and a melting point of 34-36°C. It is soluble in organic solvents and is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Due to its reactivity, it is important to handle 2-bromo-2-(m-tolyl)acetonitrile with care, following proper safety protocols.

90775-12-5

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90775-12-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 90775-12-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,7,7 and 5 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 90775-12:
(7*9)+(6*0)+(5*7)+(4*7)+(3*5)+(2*1)+(1*2)=145
145 % 10 = 5
So 90775-12-5 is a valid CAS Registry Number.

90775-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-bromo-2-(m-tolyl)acetonitrile

1.2 Other means of identification

Product number -
Other names -

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

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More Details:90775-12-5 SDS

90775-12-5Downstream Products

90775-12-5Relevant academic research and scientific papers

Enantioselective Mannich-Type Reactions to Construct Trifluoromethylthio-Containing Tetrasubstituted Carbon Stereocenters via Asymmetric Dual-Reagent Catalysis

Xu, Lijun,Wang, Hongyu,Zheng, Changwu,Zhao, Gang

supporting information, p. 2942 - 2948 (2017/09/08)

An approach to construct tetrasubstituted carbon stereocenters bearing both a trifluoromethylthio (SCF3) group and a cyano group has been realized, through asymmetric organophosphine-catalyzed Mannich-type reactions. The products were obtained

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