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3-methyl-N-[3-(trifluoromethyl)phenyl]-5,6-dihydroimidazo[2,1-b][1,3]thiazole-2-carboxamide hydrochloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64129-59-5

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64129-59-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64129-59-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,1,2 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 64129-59:
(7*6)+(6*4)+(5*1)+(4*2)+(3*9)+(2*5)+(1*9)=125
125 % 10 = 5
So 64129-59-5 is a valid CAS Registry Number.

64129-59-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-N-[3-(trifluoromethyl)phenyl]-5,6-dihydroimidazo[2,1-b][1,3]thiazole-2-carboxamide,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:64129-59-5 SDS

64129-59-5Downstream Products

64129-59-5Relevant academic research and scientific papers

Effect of Structural Change on Acute Toxicity and Antiinflammatory Activity in a Series of Imidazothiazoles and Thiazolobenzimidazoles

Powers, Larry J.,Fogt, S. W.,Ariyan, Z. S.,Rippin, D. J.,Heilman, R. D.,Matthews, Richard J.

, p. 604 - 609 (2007/10/02)

The effect of structural change on the biological activity of a series of imidazothiazoles and thiazolobenzimidazoles is described.It was found that compounds with polar substituents at the 2 or 3 position of the ring system are less acutely toxic while maintaining antiinflammatory activity.Other structural changes, such as the incorporation of a gem-dimethyl substituent in the 6 position, increase acute toxicity and eliminate antiinflammatory activity.The compound with the best activity/toxicity ratio contains an alkyl sulfonyl substituent on the thiazole ring.The thiazolobenzimidazole analogues are more potent than the imidazole analogues.

Antiinflammatory imidazothiazoles and thiazolopyrimidines

-

, (2008/06/13)

Certain imidazothiazoles and thiazolopyrimidines have been found to prevent and inhibit the formation of granuloma tissue in animals. This result is accomplished by administering to the animal subject a therapeutically effective amount of a compound havin

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