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116140-16-0

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116140-16-0 Usage

General Description

6-Methyl-3-piperidinecarboxylic acid is a chemical compound with the molecular formula C8H15NO2. It is a piperidine derivative and a carboxylic acid that contains a methyl group attached to the piperidine ring. 6-Methyl-3-piperidinecarboxylic acid is commonly used as a building block for the synthesis of various pharmaceuticals, including drugs for the treatment of central nervous system disorders and analgesics. It is also used in the production of agrochemicals and as a reagent in organic synthesis. Its unique chemical structure and properties make it a versatile compound with a wide range of applications in the pharmaceutical and agrochemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 116140-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,6,1,4 and 0 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 116140-16:
(8*1)+(7*1)+(6*6)+(5*1)+(4*4)+(3*0)+(2*1)+(1*6)=80
80 % 10 = 0
So 116140-16-0 is a valid CAS Registry Number.

116140-16-0Upstream product

116140-16-0Relevant articles and documents

PYRIMIDINE COMPOUNDS THAT INHIBIT ANAPLASTIC LYMPHOMA KINASE

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Page/Page column 161, (2011/12/02)

Compounds of Formula I are useful inhibitors of anaplastic lymphoma kinase. Compounds of Formula I have the following structure: where the definitions of the variables are provided herein.

Synthese et analyse conformationnelle de derives de l'acide nipecotique substitues par un reste methyle ou phenyle

Lapuyade, Gerard,Schlewer, Gilbert,Wermuth, Camille-Georges

, p. 663 - 668 (2007/10/02)

The synthesis and conformational analysis of methyl- or phenyl substituted nipecotic acid are reported.A chair conformation is always observed.If the configuration does permit it both the carboxylic group and the hydrocarbon substituent adopt the equatorial orientation.If a diequatorial orientation is impossible, an axial orientation is observed for the carboxylic group.

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