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156747-40-9

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156747-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 156747-40-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,6,7,4 and 7 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 156747-40:
(8*1)+(7*5)+(6*6)+(5*7)+(4*4)+(3*7)+(2*4)+(1*0)=159
159 % 10 = 9
So 156747-40-9 is a valid CAS Registry Number.

156747-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-aminopropyl)benzamide

1.2 Other means of identification

Product number -
Other names Benzamide,N-(2-aminopropyl)

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:156747-40-9 SDS

156747-40-9Downstream Products

156747-40-9Relevant articles and documents

N-acylcarbazole as a selective transamidation reagent

Kang, Bubwoong,Kuse, Masaki,Okamura, Hironori,Sakai, Asumi,Satoh, Tetsuya,Shinada, Tetsuro,Yasuno, Yoko

, p. 993 - 999 (2020/09/22)

N-acylation reaction offers an opportunity to develop an efficient synthesis of amide group-containing molecules. We found that N-acyl carbazoles showed remarkable selectivity in transamidation. Sterically less hindered primary amines are selectively acylated with N-acyl carbazoles without any additives. Various functional groups such as alcohol, phenol, indole, and aniline moieties are tolerated under mild conditions. The synthetic utility was displayed in one-pot synthesis of an N-acyl polyamine natural product. The terminal amines of spermidine were selectively benzoylated with N-benzoyl carbazole, followed by acetylation reaction accomplished the total synthesis in a highly efficient manner.

Group IV-Metal-Catalyzed Aminolysis of N-Acyl-2-oxazolidinones: Applications to the Chemoselective and Enantioselective Carbonylation of Primary Alkylamines

Yokomatsu, Tsutomu,Arakawa, Akio,Shibuya, Shiroshi

, p. 3506 - 3508 (2007/10/02)

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