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32294-42-1

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32294-42-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32294-42-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,2,9 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 32294-42:
(7*3)+(6*2)+(5*2)+(4*9)+(3*4)+(2*4)+(1*2)=101
101 % 10 = 1
So 32294-42-1 is a valid CAS Registry Number.

32294-42-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(6-methoxy-1,3-benzothiazol-2-yl)-3-phenylthiourea

1.2 Other means of identification

Product number -
Other names 1-(6-methoxybenzo[d]thiazol-2-yl)-3-phenylthiourea

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:32294-42-1 SDS

32294-42-1Relevant articles and documents

Molecular Iodine-Promoted [3 + 2] Oxidative Cyclization for the Synthesis of Heteroarene-Fused [1,2,4] Thiadiazoles/Selenadiazoles

Chen, Jin-Yu,Selvaraju, Manikandan,Lin, Yen-Tzu,Dhole, Sandip,Lin, Chih-Yu,Sun, Chung-Ming

, p. 5570 - 5579 (2020/04/20)

Two new classes of heteroarene-fused [1,2,4]thiadiazole and [1,2,4]selenadiazole are synthesized through the iodine-mediated [3 + 2] oxidative cyclization of 2-aminoheteroarenes and isothiocyanates/isoselenocyanates. This oxidative [3 + 2] annulation stra

Identification of small-molecule inhibitors of the Aβ-ABAD interaction

Xie, Yuli,Deng, Shixian,Chen, Zhenzhang,Yan, Shidu,Landry, Donald W.

, p. 4657 - 4660 (2007/10/03)

The interaction of amyloid beta peptide (Aβ) and Aβ-binding alcohol dehydrogenase (ABAD) was recently implicated in the pathogenesis of Alzheimer's disease (AD). Using an ELISA-based screening assay, we identified frentizole, an FDA-approved immunosuppressive drug, as a novel inhibitor of the Aβ-ABAD interaction. Analysis of the frentizole structure-activity relationship led to identification of a novel benzothiazole urea with a 30-fold improvement in potency.

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