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267220-58-6

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267220-58-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 267220-58-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,7,2,2 and 0 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 267220-58:
(8*2)+(7*6)+(6*7)+(5*2)+(4*2)+(3*0)+(2*5)+(1*8)=136
136 % 10 = 6
So 267220-58-6 is a valid CAS Registry Number.

267220-58-6SDS

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 1-(cyanomethyl)piperidine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Piperidinecarboxylicacid,1-(cyanomethyl)-(9CI)

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:267220-58-6 SDS

267220-58-6Downstream Products

267220-58-6Relevant articles and documents

Syntheses of R and S isomers of AF-DX 384, a selective antagonist of muscarinic M2 receptors

Martin, Juliette,Deagostino, Annamaria,Perrio, Cecile,Dauphin, Francois,Ducandas, Christophe,Morin, Christophe,Desbene, Paul-Louis,Lasne, Marie Claire

, p. 591 - 600 (2007/10/03)

Enantiomers of 5,11-dihydro-11-[2-[2-[(N,N-dipropylaminomethyl)piperidin-1-yl]ethylamino]-carbonyl]-6H-pyrido[2,3-b][1,4]benzodiazepin-6-one (AF-DX 384) 1, have been synthesized from (S)-(+) and (R)-(-)-2-[N,N-dipropylaminomethyl]piperidine 4. The enantiomeric excess of 1 has been determined by capillary electrophoresis by using the α-highly sulphated cyclodextrin (α-HSCD) as chiral selector within the running electrolyte. (S)-(+)-(4) was prepared from (S)-(-)-pipecolic acid in a 4-step procedure (overall yield: 30%, ee: 99%) and (R)-(-)-AF-DX 384 from (R)-(+)-pipecolic acid. The (R)-(-) isomer exhibited in vitro a 23-fold higher affinity than its enantiomer (S)-(+) towards muscarinic receptors of subtype 2. Copyright (C) 2000.

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