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1-Cyclohexyl-3-hydroxyurea is an organic compound with the chemical formula C7H14N2O2. It is a derivative of urea, featuring a cyclohexyl group attached to the first carbon atom and a hydroxyl group on the third carbon atom. 1-cyclohexyl-3-hydroxyurea is known for its potential applications in various fields, such as pharmaceuticals and materials science. It has been studied for its ability to inhibit certain enzymes and its potential use as a building block in the synthesis of more complex molecules. The compound is typically synthesized through chemical reactions involving cyclohexylamine and hydroxylamine, and its properties, such as solubility and reactivity, can be influenced by the presence of the cyclohexyl group, making it a subject of interest for researchers exploring its chemical behavior and possible applications.

5302-21-6

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5302-21-6 Usage

Type of compound

Organohydroxyurea derivative

Functional group

Hydroxyurea

Structural feature

Cyclohexyl group and hydroxyurea functional group attached to the same nitrogen atom

Potential applications

a. Organic synthesis
b. Pharmaceutical chemistry
c. Chelating agent
d. Antimicrobial activity
e. Antitumor activity

Versatility

Range of possible applications in the chemical and pharmaceutical industries

Check Digit Verification of cas no

The CAS Registry Mumber 5302-21-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,0 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5302-21:
(6*5)+(5*3)+(4*0)+(3*2)+(2*2)+(1*1)=56
56 % 10 = 6
So 5302-21-6 is a valid CAS Registry Number.

5302-21-6SDS

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 1-cyclohexyl-3-hydroxyurea

1.2 Other means of identification

Product number -
Other names N'-Cyclohexyl-N-hydroxy-harnstoff

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:5302-21-6 SDS

5302-21-6Relevant academic research and scientific papers

Synthesis of substituted N-hydroxyureas via the in situ generation of t-butoxy isocyanate

Krause, Josef G.,Leskiw, Brian D.,Emery, Michelle L.,McGahan, Megan E.,McCourt, Mary P.,Priefer, Ronny

body text, p. 3568 - 3570 (2010/08/07)

Treatment of primary and secondary amines with tert- butylmesitylenesulfonoxycarbamate and a base afforded tert-butoxyurea, which when treated with an acid ultimately yielded substituted N-hydroxyureas. It is proposed that this proceeded via the generation of t-butoxy isocyanate in situ. This method allows for the synthesis of both mono and disubstituted N-hydroxyureas.

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