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139285-00-0

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139285-00-0 Usage

Chemical class

Imidazole derivatives

Also known as

Methylpasaquine

Usage

Organic synthesis, pharmaceutical research

Potential applications

Antibacterial and antifungal agent, carbonic anhydrase inhibitor

Involvement in physiological processes

Carbonic anhydrase inhibition

Versatility

Potential applications in various fields of chemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 139285-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,2,8 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 139285-00:
(8*1)+(7*3)+(6*9)+(5*2)+(4*8)+(3*5)+(2*0)+(1*0)=140
140 % 10 = 0
So 139285-00-0 is a valid CAS Registry Number.

139285-00-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [1-(4-methylphenyl)sulfonylimidazol-4-yl]methanol

1.2 Other means of identification

Product number -
Other names 1-[(4-methylphenyl)sulfonyl]-4-hydroxymethylimidazole

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:139285-00-0 SDS

139285-00-0Relevant articles and documents

Structure-based design of imidazole-containing peptidomimetic inhibitors of protein farnesyltransferase

Ohkanda, Junko,Strickland, Corey L.,Blaskovich, Michelle A.,Carrico, Dora,Lockman, Jeffrey W.,Vogt, Andreas,Bucher, Cynthia J.,Sun, Jiazhi,Qian, Yimin,Knowles, David,Pusateri, Erin E.,Sebti, Said M.,Hamilton, Andrew D.

, p. 482 - 492 (2008/02/04)

A series of imidazole-containing peptidomimetic PFTase inhibitors and their co-crystal structures bound to PFTase and FPP are reported. The structures reveal that the peptidomimetics adopt a similar conformation to that of the extended CVIM tetrapeptide,

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