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1-hydroxy-3-(2-methylphenyl)urea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28788-17-2

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28788-17-2 Usage

Structure

A urea derivative containing a hydroxyl group (-OH) and a 2-methylphenyl group.

Potential applications

Medicinal chemistry, specifically in the development of new pharmaceutical drugs.

Usage

Research and laboratory settings for its properties and reactivity.

Contribution

May contribute to the advancement of scientific fields such as drug discovery and organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 28788-17-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,7,8 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 28788-17:
(7*2)+(6*8)+(5*7)+(4*8)+(3*8)+(2*1)+(1*7)=162
162 % 10 = 2
So 28788-17-2 is a valid CAS Registry Number.

28788-17-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3-(2-methylphenyl)urea

1.2 Other means of identification

Product number -
Other names Urea,N-hydroxy-N'-(2-methylphenyl)

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:28788-17-2 SDS

28788-17-2Downstream Products

28788-17-2Relevant academic research and scientific papers

N-substituted hydroxyureas as urease inhibitors

Uesato, Shinichi,Hashimoto, Yuichiro,Nishino, Masaru,Nagaoka, Yasuo,Kuwajima, Hiroshi

, p. 1280 - 1282 (2007/10/03)

In order to seek a urease inhibitor more potent than hydroxyurea (1), its alkyl- or phenyl-substituted derivatives were synthesized and evaluated for their effect on the jack bean urease. Of 16 compounds tested, m-methyl-(10) and m-methoxy-phenyl substituted hydroxyurea (13) showed the most potent inhibitory activities against the enzyme.

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