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133833-91-7

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133833-91-7 Usage

Synthesis Reference(s)

Journal of Medicinal Chemistry, 34, p. 2158, 1991 DOI: 10.1021/jm00111a035

Check Digit Verification of cas no

The CAS Registry Mumber 133833-91-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,3,8,3 and 3 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 133833-91:
(8*1)+(7*3)+(6*3)+(5*8)+(4*3)+(3*3)+(2*9)+(1*1)=127
127 % 10 = 7
So 133833-91-7 is a valid CAS Registry Number.

133833-91-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-4-hydroxythiazole

1.2 Other means of identification

Product number -
Other names 2,5-Dimethyl-thiazol-4-ol

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:133833-91-7 SDS

133833-91-7Downstream Products

133833-91-7Relevant articles and documents

4-Hydroxythiazole Inhibitors of 5-Lipoxygenase

Kerdesky, Francis A. J.,Holms, James H.,Moore, Jimmie L.,Bell, Randy L.,Dyer, Richard D.,et al.

, p. 2158 - 2165 (2007/10/02)

4-Hydroxythiazoles have been identified as potent inhibitors of 5-lipoxygenase in vitro exhibiting IC50's of less than 1 μM.An investigation of structure-activity relationships showed that the most potent inhibitors of this series are the 5-phenyl derivatives.The corresponding thiazolidin-4-one analogues were found to be relatively inactive.The 4-hydroxythiazoles were active inhibitors against 5-lipoxygenase in both intact rat polymorphonuclear leukocytes and human whole blood.The compounds were also selective inhibitors of 5-lipoxygenase, displaying only weak activity against other related enzymes, cyclooxygenase and 12- and 15-lipoxygenase.

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