116140-16-0 Usage
Uses
Used in Pharmaceutical Industry:
6-Methyl-3-piperidinecarboxylic acid is used as a building block for the synthesis of various pharmaceuticals, particularly drugs for the treatment of central nervous system disorders and analgesics. Its unique chemical structure allows it to be incorporated into the development of new medications with improved efficacy and safety profiles.
Used in Agrochemical Industry:
6-Methyl-3-piperidinecarboxylic acid is also used in the production of agrochemicals, where it serves as a key component in the synthesis of various pesticides and herbicides. Its versatility in chemical reactions enables the creation of effective and targeted agrochemicals for agricultural applications.
Used as a Reagent in Organic Synthesis:
In addition to its applications in the pharmaceutical and agrochemical industries, 6-Methyl-3-piperidinecarboxylic acid is also used as a reagent in organic synthesis. Its ability to participate in various chemical reactions makes it a valuable tool for researchers and chemists in the development of new compounds and materials.
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.
116140-16-0Relevant 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.
FARNESYL PROTEIN TRANSFERASE INHIBITORS
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Page/Page column 137, (2010/02/11)
Disclosed are compounds of formula (1.0), wherein R represents a cyclic moiety to which is bound an imodazolylalkyl group; R represents a carbamate, urea, amide or sulfonamide group; and the remaining substituents are as defined herein. Also disclosed is a method of treating cancer and a method of inhibiting farnesyl protein transferase using the disclosed compounds.
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.
