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Urea, N-butyl-N-(phenylmethyl)-N'-[3-(trifluoromethyl)phenyl]-, also known as 1-(3-trifluoromethylphenyl)-3-(phenylmethyl)butylurea, is a complex organic compound with the molecular formula C17H18F3N2O. It is a derivative of urea, featuring a butyl chain, a phenylmethyl group, and a trifluoromethylphenyl moiety. This chemical is primarily used as a pharmaceutical intermediate, specifically in the synthesis of certain drugs and agrochemicals. Its unique structure and properties make it a valuable component in the development of new compounds with potential therapeutic or pesticidal applications.

88452-29-3

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88452-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88452-29-3 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 2 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88452-29:
(7*8)+(6*8)+(5*4)+(4*5)+(3*2)+(2*2)+(1*9)=163
163 % 10 = 3
So 88452-29-3 is a valid CAS Registry Number.

88452-29-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzyl-1-butyl-3-[3-(trifluoromethyl)phenyl]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

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Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88452-29-3 SDS

88452-29-3Downstream Products

88452-29-3Relevant 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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