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25017-51-0

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25017-51-0 Usage

Chemical class

Urea derivative

Structural features

Contains a phenyl group
Contains a hydroxy group

Applications

Synthesis of pharmaceuticals
Synthesis of agrochemicals

Potential uses

Anti-inflammatory agent
Antioxidant agent

Versatility

Phenyl and hydroxy groups make it a versatile building block for the synthesis of various bioactive compounds

Additional applications

Reagent in the chemical industry
Intermediate in the production of other compounds

Check Digit Verification of cas no

The CAS Registry Mumber 25017-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,0,1 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25017-51:
(7*2)+(6*5)+(5*0)+(4*1)+(3*7)+(2*5)+(1*1)=80
80 % 10 = 0
So 25017-51-0 is a valid CAS Registry Number.

25017-51-0SDS

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 2-(4-hydroxyphenyl)ethylurea

1.2 Other means of identification

Product number -
Other names p-Hydroxy-phenaethyl-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:25017-51-0 SDS

25017-51-0Relevant articles and documents

Iron-catalyzed reaction of urea with alcohols and amines: A safe alternative for the synthesis of primary carbamates

Pe?a-López, Miguel,Neumann, Helfried,Beller, Matthias

, p. 2233 - 2238 (2017/07/25)

A general study of the iron-catalyzed reaction of urea with nucleophiles is here presented. The carbamoylation of alcohols allows for the synthesis of N-unsubstituted (primary) carbamates, including present drugs (Felbamate and Meprobamat, without the necessity to apply phosgene and related derivatives. Using amines as nucleophiles gave rise to the respective mono-and disubstituted ureas via selective transamidation reaction. These atom-economical transformations provide a direct and selective access to valuable compounds from cheap and readily available urea using a simple Lewis-acidic iron(Icatalyst.

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