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20413-07-4

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20413-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20413-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,1 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 20413-07:
(7*2)+(6*0)+(5*4)+(4*1)+(3*3)+(2*0)+(1*7)=54
54 % 10 = 4
So 20413-07-4 is a valid CAS Registry Number.

20413-07-4SDS

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 α-benzoyl-p-dimethylaminocinnamonitrile

1.2 Other means of identification

Product number -
Other names 2-benzoyl-3-(4-dimethylamino-phenyl)-acrylonitrile

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:20413-07-4 SDS

20413-07-4Relevant articles and documents

Development of Tyrphostin Analogues to Study Inhibition of the Mycobacterium tuberculosis Pup Proteasome System**

Janssen, Guido V.,Zhang, Susan,Merkx, Remco,Schiesswohl, Christa,Chatterjee, Champak,Darwin, K. Heran,Geurink, Paul P.,van der Heden van Noort, Gerbrand J.,Ovaa, Huib

, p. 3082 - 3089 (2021/09/14)

Tuberculosis is a global health problem caused by infection with the Mycobacterium tuberculosis (Mtb) bacteria. Although antibiotic treatment has dramatically reduced the impact of tuberculosis on the population, the existence and spreading of drug resist

Dienamine-Mediated Asymmetric Inverse-Electron-Demand Hetero-Diels–Alder Reaction of Linear Deconjugated Enones: Diversity-Oriented Synthesis of 3,4-Dihydropyrans

Maity, Rajendra,Pan, Subhas Chandra

supporting information, p. 871 - 874 (2017/02/15)

The first organocatalytic asymmetric inverse-electron-demand Diels–Alder reaction of deconjugated enones by using a linear dienamine was explored. Electron-poor oxadienes having a cyano group were found to be suitable in this reaction. With a 20 mol-% loa

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