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474645-92-6

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474645-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 474645-92-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,4,6,4 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 474645-92:
(8*4)+(7*7)+(6*4)+(5*6)+(4*4)+(3*5)+(2*9)+(1*2)=186
186 % 10 = 6
So 474645-92-6 is a valid CAS Registry Number.

474645-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3R)-[3-(4-trifluoromethylphenylamino)pentanoyl]carbamic acid methyl ester

1.2 Other means of identification

Product number -
Other names methyl (R)-N-[3-(4-trifluoromethyl-phenylamino)pentanoyl]carbamate

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:474645-92-6 SDS

474645-92-6Relevant articles and documents

SYNTHESIS OF IMIDE COMPOUNDS

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Page/Page column 11-13; 17-18, (2008/12/05)

The invention relates to a process for the production of an imide (1) (2) (3) via the enantioselective addition of an amine (2) to an alkene (3) wherein Y is OR, wherein R is alkyl or Bn, said process comprising: incubating Pd(OTf)2 with a phos

Asymmetric synthesis of the cholesteryl ester transfer protein inhibitor torcetrapib

Damon, David B.,Dugger, Robert W.,Hubbs, Stephen E.,Scott, Jill M.,Scott, Robert W.

, p. 472 - 480 (2012/12/22)

Previously our group reported synthetic efforts used to synthesize kilogram quantities of the cholesteryl ester transfer protein (CETP) inhibitor torcetrapib, 1, via a mid-stage resolution. This account describes research conducted to develop an asymmetri

Method for producing (R) -3- [4- (trifluoromethyl) phenylamino] -pentanoic acid amide derivative

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Page 18, (2010/02/08)

The present invention provides a method for easily producing an (R)-3-[4-(trifluoromethyl)phenylamino]-pentanoic acid amide derivative useful for an intermediate for pharmaceutical products, particularly an inhibitor of a cholesteryl ester transfer protei

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