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3028-04-4

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3028-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3028-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,2 and 8 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3028-04:
(6*3)+(5*0)+(4*2)+(3*8)+(2*0)+(1*4)=54
54 % 10 = 4
So 3028-04-4 is a valid CAS Registry Number.

3028-04-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,3-benzothiazol-2-yl)-2-methylpropanamide

1.2 Other means of identification

Product number -
Other names N-Benzothiazol-2-yl-isobutyramide

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:3028-04-4 SDS

3028-04-4Relevant articles and documents

Fragment-based design of selective GPCR ligands guided by free energy simulations

Matricon, Pierre,Vo, Duc Duy,Gao, Zhan-Guo,Kihlberg, Jan,Jacobson, Kenneth A.,Carlsson, Jens

supporting information, p. 12305 - 12308 (2021/12/07)

Fragment-based drug discovery relies on successful optimization of weakly binding ligands for affinity and selectivity. Herein, we explored strategies for structure-based evolution of fragments binding to a G protein-coupled receptor. Molecular dynamics s

Aerobic Copper-Mediated Domino Three-Component Approach to 2-Aminobenzothiazole Derivatives

Castanheiro, Thomas,Suffert, Jean,Gulea, Mihaela,Donnard, Morgan

supporting information, p. 2588 - 2591 (2016/06/15)

An unprecedented three-component reaction involving a 2,2′-diaminodiaryl disulfide, copper cyanide, and an electrophile is described. This transformation is based on an oxidative copper-mediated S-cyanation as a key step and involves a cyanation/cyclization/acylation domino sequence enabling a rapid and efficient synthesis of diversely substituted 2-aminobenzothiazole derivatives. Notably, this reaction proceeds via an original mechanism involving an intermolecular migration of the acyl group.

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