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123772-37-2

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123772-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 123772-37-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,3,7,7 and 2 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 123772-37:
(8*1)+(7*2)+(6*3)+(5*7)+(4*7)+(3*2)+(2*3)+(1*7)=122
122 % 10 = 2
So 123772-37-2 is a valid CAS Registry Number.

123772-37-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-6-p-chlorophenylimidazo<2,1-b>thiazole-5-carboxaldehyde

1.2 Other means of identification

Product number -
Other names 6-(4-Chloro-phenyl)-2-methyl-imidazo[2,1-b]thiazole-5-carbaldehyde

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:123772-37-2 SDS

123772-37-2Relevant articles and documents

Human constitutive androstane receptor agonist DL5016: A novel sensitizer for cyclophosphamide-based chemotherapies

Liang, Dongdong,Li, Linhao,Lynch, Caitlin,Mackowiak, Bryan,Hedrich, William D.,Ai, Yong,Yin, Yue,Heyward, Scott,Xia, Menghang,Wang, Hongbing,Xue, Fengtian

, p. 84 - 99 (2019/06/27)

The DNA alkylating prodrug cyclophosphamide (CPA), alone or in combination with other agents, is one of the most commonly used anti-cancer agents. As a prodrug, CPA is activated by cytochrome P450 2B6 (CYP2B6), which is transcriptionally regulated by the

Imidazothiazole Carbamates and Acylureas as Potential Insect Control Agents

Andreani, Aldo,Rambaldi, Mirella,Carloni, Patricia,Greci, Lucedio,Stipa, Pierluigi

, p. 525 - 529 (2007/10/02)

Imidazothiazole carbamates and acylureas were prepared by reaction of 5-hydroxymethylimidazothiazole and imidazothiazole-5-carboxyamide with arylisocyanates.The products formed depend from the substituent bonded at the 6 position of t

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