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1-hydroxy-3-propylurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

5710-12-3

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5710-12-3 Usage

Potential pharmaceutical applications

cancer and diabetes treatment

Potential agricultural applications

herbicide, fungicide, and plant growth enhancer
Ongoing research and investigation for diverse range of potential applications

Check Digit Verification of cas no

The CAS Registry Mumber 5710-12-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,1 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5710-12:
(6*5)+(5*7)+(4*1)+(3*0)+(2*1)+(1*2)=73
73 % 10 = 3
So 5710-12-3 is a valid CAS Registry Number.

5710-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-hydroxy-3-propylurea

1.2 Other means of identification

Product number -
Other names N-Propylcarbamoyl-hydroxylamin

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:5710-12-3 SDS

5710-12-3Upstream product

5710-12-3Downstream Products

5710-12-3Relevant 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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