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141083-85-4

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141083-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 141083-85-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,8 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 141083-85:
(8*1)+(7*4)+(6*1)+(5*0)+(4*8)+(3*3)+(2*8)+(1*5)=104
104 % 10 = 4
So 141083-85-4 is a valid CAS Registry Number.

141083-85-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2,3,6-tetra-hydro-2-pyridinecarboxylic acid methyl ester

1.2 Other means of identification

Product number -
Other names 1,2,3,6-tetrahydropyridine-2-carboxylic acid methyl 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:141083-85-4 SDS

141083-85-4Relevant articles and documents

SELECTIVE FKBP51 LIGANDS FOR TREATMENT OF PSYCHIATRIC DISORDERS

-

, (2015/04/15)

The present invention relates to compounds of the general formula (I) having a selective FKBP51 ligand scaffold, pharmaceutically acceptable salts of these compounds and pharmaceutical compositions containing at least one of these compounds together with

A ring-closing metathesis-mediated route to novel enantiopure conformationally restricted cyclic amino acids

Tjen, Kim C. M. F.,Kinderman, Sape S.,Schoemaker, Hans E.,Hiemstra, Henk,Rutjes, Floris P. J. T.

, p. 699 - 700 (2007/10/03)

A combination of palladium-catalysed N,O-acetal formation, ruthenium- catalysed ring-closing metathesis and N-sulfonyliminium ion-mediated C-C bond formation constitutes an efficient and versatile route to a set of enantiomerically pure 2,6-disubstituted unsaturated pipecolic acid derivatives.

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