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14202-55-2

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14202-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14202-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,2,0 and 2 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14202-55:
(7*1)+(6*4)+(5*2)+(4*0)+(3*2)+(2*5)+(1*5)=62
62 % 10 = 2
So 14202-55-2 is a valid CAS Registry Number.

14202-55-2SDS

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 N-heptylacetamide

1.2 Other means of identification

Product number -
Other names N-heptyl-acetamide

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:14202-55-2 SDS

14202-55-2Downstream Products

14202-55-2Relevant articles and documents

Tandem synthesis of amides and secondary amines from esters with primary amines under solvent-free conditions

Lee, Jeongbin,Muthaiah, Senthilkumar,Hong, Soon Hyeok

, p. 2653 - 2660 (2014/09/17)

An iridium(III)-catalyzed tandem synthesis of amides and amines from esters under solvent-free conditions is described. A commercially available iridium(III) complex, [Cp*IrCl2]2, with sodium acetate showed the best activity for the synthesis of amides and secondary amines. The amide was formed by ester-amide exchange which generates an alcohol in situ which is subsequently transformed to a secondary amine via hydrogen autotransfer. This synthetic protocol with high atom economy generates water as the sole by-product and can afford amides and amines from various esters in a one-pot reaction, expanding the synthetic versatility of ester transformations.

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