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282527-19-9

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282527-19-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 282527-19-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,2,5,2 and 7 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 282527-19:
(8*2)+(7*8)+(6*2)+(5*5)+(4*2)+(3*7)+(2*1)+(1*9)=149
149 % 10 = 9
So 282527-19-9 is a valid CAS Registry Number.

282527-19-9SDS

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 (2S,6S)-6-prop-2-ynyl-1,2,3,6-tetrahydropyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylicacid,1,2,3,6-tetrahydro-6-(2-propyn-1-yl)-,(2S,6S)

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:282527-19-9 SDS

282527-19-9Downstream Products

282527-19-9Relevant articles and documents

Ring-closing metathesis of allylic O,O- and N,O-acetals

Kinderman, Sape S.,Doodeman, Robin,Van Beijma, Jetze W.,Russcher, Jaap C.,Tjen, Kim C. M. F.,Kooistra, T. Martijn,Mohaselzadeh, Homayun,Van Maarseveen, Jan H.,Hiemstra, Henk,Schoemaker, Hans E.,Rutjes, Floris P. J. T.

, p. 736 - 748 (2007/10/03)

A variety of allylic O,O- and N,O-acetals were synthesized using a mild palladium-catalyzed coupling of an alcohol or sulfonamide with an alkyl or aryl 1,2-propadienyl ether. The resulting linear acetals were used for the synthesis of unsaturated rings via ring-closing metathesis, in which the acetal carbon-a precursor for oxycarbenium or N-sulfonyliminium ions, respectively-served as a reactive center for further introduction of functional groups. The products-unsaturated oxygen and nitrogen heterocyclic scaffolds - offer multiple opportunities for derivatization as illustrated with the synthesis of substituted dihydropyrans, chromenes, enantiopure tetrahydropyridines and an enantiomerically pure quinolizidine amino acid.

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