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Urea, N-hydroxy-N'-(phenylmethyl)-, also known as N-hydroxy-N'-(phenylmethyl)urea or N-hydroxy-N'-benzylurea, is an organic compound with the chemical formula C8H10N2O2. It is a derivative of urea, where one hydrogen atom is replaced by a phenylmethyl group (C6H5CH2-). Urea, N-hydroxy-N'-(phenylmethyl)- is a white crystalline solid and is used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. It is also known for its potential applications in the field of materials science, such as in the development of polymers and coatings. The compound is synthesized through various methods, including the reaction of urea with benzyl chloride in the presence of a base. Due to its reactivity, it is often used in the preparation of other compounds, making it a valuable building block in organic chemistry.

24966-37-8

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24966-37-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24966-37-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,6 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 24966-37:
(7*2)+(6*4)+(5*9)+(4*6)+(3*6)+(2*3)+(1*7)=138
138 % 10 = 8
So 24966-37-8 is a valid CAS Registry Number.

24966-37-8SDS

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-benzyl-3-hydroxyurea

1.2 Other means of identification

Product number -
Other names 1-hydroxy-3-benzylurea

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:24966-37-8 SDS

24966-37-8Relevant academic research and scientific papers

Different reactivity of hydroxylamine with carbamoyl azides and carbamoyl cyanides: Synthesis of hydroxyureas and carbamoyl amidoximes

Paz, Jairo,Perez-Balado, Carlos,Iglesias, Beatriz,Munoz, Luis

supporting information; experimental part, p. 8039 - 8047 (2011/02/26)

The carbamoylating agents carbamoyl azides and carbamoyl cyanides (aka cyanoformamides) react with hydroxylamine in different ways, leading in the first case to N-hydroxyureas and, in the case of carbamoyl cyanides, to carbamoyl amidoxime derivatives. The

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.

A convenient method for the synthesis of N-hydroxyureas

Parrish, Dennis A.,Zou, Zhou,Allen, C. Leigh,Day, Cynthia S.,King, S. Bruce

, p. 8841 - 8843 (2007/10/03)

Treatment of amines with 1-(4-nitrophenol)-N-(O-benzylhydroxy)carbamate yields the O-benzyl protected N-hydroxyureas. Hydrogenation of the O-benzyl protected N-hydroxyureas over 5% Pd/BaSO4 cleanly gives the N-hydroxyureas in good yield. In add

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