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222960-38-5

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222960-38-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222960-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,9,6 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 222960-38:
(8*2)+(7*2)+(6*2)+(5*9)+(4*6)+(3*0)+(2*3)+(1*8)=125
125 % 10 = 5
So 222960-38-5 is a valid CAS Registry Number.

222960-38-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-aminoethoxy)benzamide

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:222960-38-5 SDS

222960-38-5Relevant articles and documents

Novel approach to the synthesis of istaroxime

Liang,Guo,Jiang

, p. 2643 - 2647 (2017/12/26)

Istaroxime 1, a novel cardiotonic agent with high efficiency and low toxicity was synthesized from dehydroepiandrosterone 2 using a novel approach that included epoxidation, ring-opening, substitution, and oximation. The new protocol without gas protection was milder than the reported approaches. The overall yield of the method was 24.1%.

AN IMPROVED SYNTHETIC ROUTE TO AMONOXYPROPYLAMINE (APA) AND RELATED HOMOLOGS

Pankaskie, Marvin C.,Scholtz, Stephen A.

, p. 339 - 344 (2007/10/02)

Aminoxypropylamine (APA) has been found to be a potent inhibitor of several enzymatic pathways involved in the biosynthesis of the naturally occuring polyamines putrescine, spermidine, and spermine.This report describes a convenient, three-step synthesis of APA, as well as its ethyl and butyl homologs, utilizing starting materials and intermediates useful in the preparation of other related aminoxyalkylamines.

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