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30085-34-8

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30085-34-8 Usage

General Description

1-(4-chlorophenyl)-3-hydroxyurea is a chemical compound with the formula C7H8ClN3O2. It is a derivative of hydroxyurea, which is used in the treatment of various types of cancer and sickle cell disease. 1-(4-chlorophenyl)-3-hydroxyurea has been studied for its potential anticancer and antiproliferative activities. It has also been investigated for its potential use as an anti-inflammatory and immunomodulatory agent. Additionally, this compound has been researched for its potential to inhibit the growth of certain types of bacteria and fungi. Further research is needed to fully understand the potential therapeutic applications of 1-(4-chlorophenyl)-3-hydroxyurea.

Check Digit Verification of cas no

The CAS Registry Mumber 30085-34-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,0,8 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 30085-34:
(7*3)+(6*0)+(5*0)+(4*8)+(3*5)+(2*3)+(1*4)=78
78 % 10 = 8
So 30085-34-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7ClN2O2/c8-5-1-3-6(4-2-5)9-7(11)10-12/h1-4,12H,(H2,9,10,11)

30085-34-8SDS

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-chlorophenyl)-3-hydroxyurea

1.2 Other means of identification

Product number -
Other names N'-Hydroxy-N-<4-chlor-phenyl>-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:30085-34-8 SDS

30085-34-8Relevant articles and documents

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.

REACTION OF TRISUBSTITUTED UREAS WITH AMINO-CONTAINING COMPOUNDS

Veis, I.,Ruff, E.,Otvosh, L.

, p. 694 - 696 (2007/10/02)

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