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130804-35-2

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  • 3-(2,4-difluorophenyl)-1-[5-[[4,5-di(phenyl)-1H-imidazol-2-yl]sulfanyl]pentyl]-1-heptylurea

    Cas No: 130804-35-2

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130804-35-2 Usage

Uses

Antihyperlipidemic.

Check Digit Verification of cas no

The CAS Registry Mumber 130804-35-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,8,0 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 130804-35:
(8*1)+(7*3)+(6*0)+(5*8)+(4*0)+(3*4)+(2*3)+(1*5)=92
92 % 10 = 2
So 130804-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C34H40F2N4OS/c1-2-3-4-5-13-22-40(34(41)37-30-21-20-28(35)25-29(30)36)23-14-8-15-24-42-33-38-31(26-16-9-6-10-17-26)32(39-33)27-18-11-7-12-19-27/h6-7,9-12,16-21,25H,2-5,8,13-15,22-24H2,1H3,(H,37,41)(H,38,39)

130804-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(2,4-difluorophenyl)-1-[5-[(4,5-diphenyl-1H-imidazol-2-yl)sulfanyl]pentyl]-1-heptylurea

1.2 Other means of identification

Product number -
Other names N'-(2,4-difluorophenyl)-N-[5-(4,5-diphenyl-1H-imidazol-2-ylthio)pentyl]-N-heptylurea

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:130804-35-2 SDS

130804-35-2Downstream Products

130804-35-2Relevant articles and documents

Acyl CoA:cholesterol acyltransferase (ACAT) inhibitors: Synthesis and structure-activity relationship studies of a new series of trisubstituted imidazoles

Higley,Wilde,Maduskuie,Johnson,Pennev,Billheimer,Robinson,Gillies,Wexler

, p. 3511 - 3522 (2007/10/02)

A series of 4,5-diaryl-2-(substituted thio)-1H-imidazoles has been synthesized and demonstrated to be potent inhibitors of acyl-CoA:cholesterol acyltransferase (ACAT). The design, synthesis, and structure-activity relationships for this series are reporte

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