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Urea, N-butyl-N'-(5-chloro-2-methoxyphenyl)-N-(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 synthesis of microtubules in the nematode's cells, leading to the disruption of their growth and reproduction. This chemical is effective against a wide range of nematode species and is considered safe for use in animals, with minimal side effects.

88451-17-6

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88451-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88451-17-6 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, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 88451-17:
(7*8)+(6*8)+(5*4)+(4*5)+(3*1)+(2*1)+(1*7)=156
156 % 10 = 6
So 88451-17-6 is a valid CAS Registry Number.

88451-17-6SDS

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-(5-chloro-2-methoxyphenyl)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:88451-17-6 SDS

88451-17-6Downstream Products

88451-17-6Relevant 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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