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1-(4-chlorophenyl)-3-hydroxyurea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 30085-34-8 Structure
  • Basic information

    1. Product Name: 1-(4-chlorophenyl)-3-hydroxyurea
    2. Synonyms: 1-(4-chlorophenyl)-3-hydroxyurea
    3. CAS NO:30085-34-8
    4. Molecular Formula: C7H7ClN2O2
    5. Molecular Weight: 186.59568
    6. EINECS: 250-037-3
    7. Product Categories: N/A
    8. Mol File: 30085-34-8.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: °Cat760mmHg
    3. Flash Point: °C
    4. Appearance: /
    5. Density: 1.501g/cm3
    6. Refractive Index: 1.66
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(4-chlorophenyl)-3-hydroxyurea(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-chlorophenyl)-3-hydroxyurea(30085-34-8)
    11. EPA Substance Registry System: 1-(4-chlorophenyl)-3-hydroxyurea(30085-34-8)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 30085-34-8(Hazardous Substances Data)

30085-34-8 Usage

Derivative of

Hydroxyurea

Used for

Treatment of various types of cancer and sickle cell disease

Studied for

Potential anticancer and antiproliferative activities

Investigated for

Anti-inflammatory and immunomodulatory properties

Researched for

Inhibition of growth of certain types of bacteria and fungi

Further research 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.

α-Haloalkyl Haloformates and Related Compounds 3.1 A Facile Synthesis of Symmetrical and Unsymmetrical Ureas via Chloromethyl Carbamates

Patonay, Tamas,Patonay-Peli, Erzsebet,Zolnai, Laszlo,Mogyorodi, Ferenc

, p. 4253 - 4265 (2007/10/03)

Chloromethyl carbamates were prepared by the reaction of chloromethyl chloroformates with amines and found to produce mono-, symmetrically or unsymmetrically di- and trisubstituted ureas including their N-hydroxy and N-alkoxy derivatives in moderate to good yield.

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