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Urea, N-(4-methoxyphenyl)-N'-(phenylmethoxy)-, also known as 1-(4-methoxyphenyl)-3-(phenylmethoxy)urea, is an organic compound with the molecular formula C15H16N2O3. It is a derivative of urea, featuring a 4-methoxyphenyl group attached to the nitrogen atom and a phenylmethoxy group attached to the other nitrogen atom. Urea, N-(4-methoxyphenyl)-N'-(phenylmethoxy)- is characterized by its white crystalline appearance and is soluble in organic solvents. It has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound's properties, such as its melting point, solubility, and stability, make it a valuable intermediate in the development of various chemical products.

51457-93-3

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51457-93-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51457-93-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,5 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 51457-93:
(7*5)+(6*1)+(5*4)+(4*5)+(3*7)+(2*9)+(1*3)=123
123 % 10 = 3
So 51457-93-3 is a valid CAS Registry Number.

51457-93-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-methoxyphenyl)-N'-phenylmethoxyurea

1.2 Other means of identification

Product number -
Other names N-(benzyloxy)-N'-(p-methoxyphenyl)urea

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:51457-93-3 SDS

51457-93-3Relevant academic research and scientific papers

Synthesis of 3-hydroxypyrimidine-2,4-diones. Addition of anilines to benzyloxy isocyanate synthons to give N-hydroxyureas

Romine,Martin,Meanwell,Epperson

, p. 846 - 850 (1994)

A new method, the addition of N-benzyloxychloroformate to methyl anthranilate followed by base-catalyzed cyclization, has been employed to synthesize the N-hydroxyquinazolinedione 1 and heterocyclic derivatives. N-Benzyloxycarbonylimidazole is a useful sy

N-substituted hydroxyureas as urease inhibitors

Uesato, Shinichi,Hashimoto, Yuichiro,Nishino, Masaru,Nagaoka, Yasuo,Kuwajima, Hiroshi

, p. 1280 - 1282 (2007/10/03)

In order to seek a urease inhibitor more potent than hydroxyurea (1), its alkyl- or phenyl-substituted derivatives were synthesized and evaluated for their effect on the jack bean urease. Of 16 compounds tested, m-methyl-(10) and m-methoxy-phenyl substituted hydroxyurea (13) showed the most potent inhibitory activities against the enzyme.

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