1044591-98-1

Basic information

• Product Name: (R)-3-methoxycarbonyl-(R)-5-methylpiperidine
• Synonyms: (R)-3-methoxycarbonyl-(R)-5-methylpiperidine
• CAS NO: 1044591-98-1
• Molecular Weight: 157.213
• Mol File: 1044591-98-1.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: (R)-3-methoxycarbonyl-(R)-5-methylpiperidine(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-methoxycarbonyl-(R)-5-methylpiperidine(1044591-98-1)
• EPA Substance Registry System: (R)-3-methoxycarbonyl-(R)-5-methylpiperidine(1044591-98-1)

Safety Data

• Hazardous Substances Data: 1044591-98-1(Hazardous Substances Data)

Usage

General Description

(R)-3-methoxycarbonyl-(R)-5-methylpiperidine is a chemical compound with the molecular formula C9H17NO2. It is a piperidine derivative containing a methoxycarbonyl group and a methyl substituent on the piperidine ring. (R)-3-methoxycarbonyl-(R)-5-methylpiperidine is used in the pharmaceutical industry for the synthesis of various drugs, particularly those targeting the central nervous system. It has also been studied for its potential use as a chiral building block in organic synthesis. As a chiral compound, it exhibits optical activity, and its enantiomers may have different pharmacological properties. Further research and development of this compound may lead to new pharmaceuticals and chemical products.

Upstream product

• 29681-44-5 5-bromo-3-pyridine carboxylic acid methyl ester 
• 29681-45-6 5-methylnicotinic acid methyl ester 

Downstream Products

• 1365887-45-1 1-(tert-butoxycarbonyl)-5-methylpiperidine-3-carboxylic acid 
• 1365887-44-0 1-(tert-butyl) 3-methyl 5-methylpiperidine-1,3-dicarboxylate 
• 1366053-19-1 1-(2-fluorobenzyl)-5-methylpiperidine-3-carboxylic acid 
• 1366052-54-1 N-(1-(2-fluorobenzyl)-5-methylpiperidin-3-yl)-3-(pyridin-4-yl)-6,7-dihydro-1H-pyrazolo[4,3-c]pyridine-5(4H)-carboxamide 
• 1269757-29-0 (3R,5R)-/(3S,5S)-1-(benzyloxycarbonyl)-5-methylpiperidine-3-carboxylic acid 
• 1269757-29-0 (3R,5S)-/(3S,5R)-1-(benzyloxycarbonyl)-5-methylpiperidine-3-carboxylic acid 

Relevant articles and documents

1,5-Substituted nipecotic amides: Selective PDE8 inhibitors displaying diastereomer-dependent microsomal stability

The first highly potent and selective PDE8 inhibitors are disclosed. The initial tetrahydroisoquinoline hit was transformed into a nipecotic amide series in order to address a reactive metabolite issue. Reduction of lipophilicity to address metabolic liab

PYRAZINYLPYRIDINES USEFUL FOR THE TREATMENT OF PROLIFERATIVE DISEASES

The present invention provides a compound of Formula (I) and pharmaceutically acceptable salts thereof. Also provided is a method of using a compound of Formula I for treating a disease or condition mediated by a CDK inhibitor.

HETEROARYL COMPOUNDS AS KINASE INHIBITORS

The present invention provides a compound of Formula (I): and pharmaceutically acceptable salts thereof. Also provided is a method of using a compound of Formula I for treating a disease or condition mediated by a CDK inhibitor