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198493-28-6

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  • Carbamic acid, [(1R)-1-(cyanomethyl)propyl]-, 1,1-dimethylethyl ester

    Cas No: 198493-28-6

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198493-28-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 198493-28-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,8,4,9 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 198493-28:
(8*1)+(7*9)+(6*8)+(5*4)+(4*9)+(3*3)+(2*2)+(1*8)=196
196 % 10 = 6
So 198493-28-6 is a valid CAS Registry Number.

198493-28-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-butyl N-[(2R)-1-cyanobutan-2-yl]carbamate

1.2 Other means of identification

Product number -
Other names Carbamic acid,[(1R)-1-(cyanomethyl)propyl]-,1,1-dimethylethyl ester

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:198493-28-6 SDS

198493-28-6Relevant articles and documents

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 (2006)

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

Synthesis of homochiral N-Boc-β-aminoaldehydes from N-Boc-β-aminonitriles

Toujas, Jean-Louis,Jost, Eric,Vaultier, Michel

, p. 713 - 718 (2007/10/03)

Enantiopure N-Boc-β-aminoaldehydes are efficiently prepared in good yields from N-Boc-β-aminonitriles by reduction of the nitrile function with diisobutylaluminium hydride (DIBAL-H) - Keywords: β-aminoaldehyde; β-aminonitrile; α-aminoacid; homochiral; enantiomeric excess; reduction; DIBAL-H

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