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Urea, N'-[4-(methylthio)phenyl]-N,N-bis(phenylmethyl)-, also known as Fenbendazole, is a broad-spectrum anthelmintic chemical belonging to the benzimidazole class. It is primarily used in veterinary medicine to treat and control various gastrointestinal nematode infections in livestock, including cattle, sheep, and pigs. Fenbendazole works by inhibiting the energy metabolism of the parasites, leading to their paralysis and eventual death. The chemical has a molecular formula of C16H15N3OS and is characterized by its white to off-white crystalline appearance. Due to its effectiveness and low toxicity, Fenbendazole is widely used in the agriculture and livestock industry to improve animal health and productivity.

86764-40-1

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86764-40-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86764-40-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,7,6 and 4 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 86764-40:
(7*8)+(6*6)+(5*7)+(4*6)+(3*4)+(2*4)+(1*0)=171
171 % 10 = 1
So 86764-40-1 is a valid CAS Registry Number.

86764-40-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1-dibenzyl-3-(4-methylsulfanylphenyl)urea

1.2 Other means of identification

Product number -
Other names Urea,N'-[4-(methylthio)phenyl]-N,N-bis(phenylmethyl)

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:86764-40-1 SDS

86764-40-1Downstream Products

86764-40-1Relevant 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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