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Urea, N-butyl-N'-(3-methylphenyl)-N-(phenylmethyl)-, also known as 1-(3-methylphenyl)-3-(phenylmethyl)-1-butylurea, is an organic compound with the chemical formula C18H22N2O. It is a derivative of urea, featuring a butyl group, a 3-methylphenyl group, and a phenylmethyl group attached to the urea molecule. Urea, N-butyl-N'-(3-methylphenyl)-N-(phenylmethyl)- is primarily used as a chemical intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for the formation of different chemical bonds and reactions, making it a versatile building block in the creation of complex molecules.

88451-08-5

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88451-08-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88451-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,4,5 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 88451-08:
(7*8)+(6*8)+(5*4)+(4*5)+(3*1)+(2*0)+(1*8)=155
155 % 10 = 5
So 88451-08-5 is a valid CAS Registry Number.

88451-08-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1-butyl-3-(3-methylphenyl)urea

1.2 Other means of identification

Product number -
Other names -

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:88451-08-5 SDS

88451-08-5Downstream Products

88451-08-5Relevant academic research and scientific papers

Potential Antiatherosclerotic Agents. 6. Hypocholesterolemic Trisubstituted Urea Analogues

DeVries, Vern G.,Bloom, Jonathan D.,Dutia, Minu D.,Katocs, Andrew S.,Largis, Elwood E.

, p. 2318 - 2325 (2007/10/02)

The discovery that a series of N,N-dialkyl-N'-arylureas were inhibitors of the ACAT enzyme has led to a structure-activity study involving the systematic modification of three sites of the urea backbone.This study culminated in the selection of N'-(2,4-dimethylphenyl)-N-benzyl-N-n-butylurea (115) for more extensive biological evaluation.ACAT inhibitors are seen as potentially beneficial agents against hypercholesterolemia and atherosclerosis.

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