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312747-21-0

312747-21-0

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312747-21-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312747-21-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,7,4 and 7 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 312747-21:
(8*3)+(7*1)+(6*2)+(5*7)+(4*4)+(3*7)+(2*2)+(1*1)=120
120 % 10 = 0
So 312747-21-0 is a valid CAS Registry Number.

312747-21-0 Well-known Company Product Price

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  • Sigma

  • (SML1129)  HUP30  ≥98% (HPLC)

  • 312747-21-0

  • SML1129-5MG

  • 858.78CNY

  • Detail

  • Sigma

  • (SML1129)  HUP30  ≥98% (HPLC)

  • 312747-21-0

  • SML1129-25MG

  • 3,473.73CNY

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312747-21-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-nitro-1,3-benzothiazol-2-yl)cyclohexanecarboxamide

1.2 Other means of identification

Product number -
Other names F0327-0054

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:312747-21-0 SDS

312747-21-0Downstream Products

312747-21-0Relevant articles and documents

Synthesis and biological evaluation of a series of (Benzo[d]thiazol-2-yl) cyclohexanecarboxamides and (Benzo[d]thiazol-2-yl)cyclohexanecarbothioamides

Nam, Nguyen Hai,Dung, Phan Thi Phuong,Thuong, Phuong Thien,Hien, Tran Thi

experimental part, p. 159 - 164 (2011/08/10)

A series of benzothiazole derivatives including N-(benzo[d]thiazol-2-yl) cyclohexanecarboxamides (2a-g) and N-(benzo[d]thiazol-2-yl) cyclohexancarbothioamides (3b-d) have been synthesized and evaluated for cytotoxic and antimicrobial activities. Two compo

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