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396131-82-1

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396131-82-1 Usage

Uses

3-(Cyanomethyl)benzeneboronic acid pinacol ester is used as pharmaceutical intermediate.

Check Digit Verification of cas no

The CAS Registry Mumber 396131-82-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,9,6,1,3 and 1 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 396131-82:
(8*3)+(7*9)+(6*6)+(5*1)+(4*3)+(3*1)+(2*8)+(1*2)=161
161 % 10 = 1
So 396131-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C14H18BNO2/c1-13(2)14(3,4)18-15(17-13)12-7-5-6-11(10-12)8-9-16/h5-7,10H,8H2,1-4H3

396131-82-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H52618)  3-(Cyanomethyl)benzeneboronic acid pinacol ester, 96%   

  • 396131-82-1

  • 250mg

  • 353.0CNY

  • Detail
  • Alfa Aesar

  • (H52618)  3-(Cyanomethyl)benzeneboronic acid pinacol ester, 96%   

  • 396131-82-1

  • 1g

  • 1129.0CNY

  • Detail

396131-82-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Cyanomethylphenylboronic acid, pinacol ester

1.2 Other means of identification

Product number -
Other names 3-(Cyanomethyl)phenylboronic acid,pinacol ester

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:396131-82-1 SDS

396131-82-1Downstream Products

396131-82-1Relevant articles and documents

Radical Metal-Free Borylation of Aryl Iodides

Pinet, Sandra,Liautard, Virginie,Debiais, Mégane,Pucheault, Mathieu

, p. 4759 - 4768 (2017/10/03)

A simple metal-free borylation of aryl iodides mediated by a fluoride sp 2 -sp 3 diboron adduct is described. The reaction conditions are compatible with various functional groups. Electronic effects of substituents do not affect the borylation while steric hindrance does. The reaction proceeds via a radical mechanism in which pyridine serves to stabilize the boryl radicals, generated in situ.

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