19999-64-5

Usage

Uses

Used in Pharmaceutical Industry:
1-Methylpiperidine-3-carboxylic acid hydrochloride is used as a building block for the synthesis of pharmaceuticals. Its versatile reactivity allows for the creation of a wide range of drug molecules, contributing to the development of new medications and therapies.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Methylpiperidine-3-carboxylic acid hydrochloride is used as a key component in the synthesis of various agrochemicals. Its incorporation into these products helps in the development of effective solutions for agricultural applications, such as pesticides and herbicides.
Used in Organic Chemistry Research:
1-Methylpiperidine-3-carboxylic acid hydrochloride is used as a research compound in the field of organic chemistry. Its unique properties and reactivity make it an important tool for studying chemical reactions and exploring new synthetic pathways.
Used in Drug Development:
In drug development, 1-Methylpiperidine-3-carboxylic acid hydrochloride is used as a starting material for the synthesis of potential drug candidates. Its presence in the molecular structure can influence the pharmacological properties of the final drug, making it a valuable asset in the search for new therapeutic agents.
Safety Considerations:
It is important to handle 1-Methylpiperidine-3-carboxylic acid hydrochloride with care and follow proper safety protocols due to its potential hazards and risks. This ensures the safety of those working with the compound and minimizes any adverse effects on the environment.

InChI:InChI=1/C7H13NO2.ClH/c1-8-4-2-3-6(5-8)7(9)10;/h6H,2-5H2,1H3,(H,9,10);1H

Upstream product

• 50-00-0 formaldehyd 
• 498-95-3 nipecotic acid 
• 117704-88-8 ethyl 4-diisopropylaminobutyrate 
• 2969-81-5 Ethyl 4-bromobutyrate 
• 24252-37-7 ethyl 1-methylisonipecotate 

Downstream Products

• 1018895-14-1 N-(2-fluoro-3-nitrophenyl)-1-methylpiperidine-3-carboxamide 

Relevant academic research and scientific papers

Carbostyril derivative

Carbostyril compounds or salts thereof of the formula STR1 wherein A is a C1 -C6 alkylene group; R1 is a C3 -C8 cycloalkyl-C1 -C6 alkyl group which may have, as a substituent, a

Pyrrole derivatives, their preparation and pharmaceutical compositions which contain them

This invention relates to pyrrole derivatives of formula: STR1 in which A forms with the pyrrole ring an isoindoline, 6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine, 2,3,6,7-tetrahydro-5H-[1,4]oxathiino[2,3-c]pyrrole or 2,3,6,7-tetrahydro-5H-[1,4]dithiino[2,3-c]pyrrole ring-system and Hetis naphthyridinyl, pyridyl or quinolyl which is unsubstituted or substituted with halogen, (1 to 4 C) alkyl, (1 to 4 C) alkyloxy, (1 to 4 C) alkylthio or CF3 and R=(3 to 10 C) straight- or branched-chain alkenyl or alkyl which is unsubstituted or substituted with alkyloxy, alkylthio, (3 to 6 C) cycloalkyl, NH2, alkylamino, dialkylamino, alkylcarbonylamino, (in which the amino portion is optionally substituted with alkyl), 1- or 2-piperazinyl, piperidyl, piperidino, morpholino, pyrrolidinyl, 1-azetidinyl, carbamoyl, alkylcarbamoyl, dialkylcarbamoyl, (1-piperazinyl)carbonyl, piperidinocarbonyl, (1-pyrrolidinyl)carbonyl, phenyl, pyridyl, 1-imidazolyl, or alternatively R=2- or 3-pyrrolidinyl, 2-, 3- or 4-piperidyl, on the understanding that the alkyl radicals are straight- or branched-chain radicals and contain, except where specifically stated, 1 to 10 C, and that the piperazinyl, piperidino, piperidyl, pyrrolidinyl and azetidinyl radicals can be unsubstituted or substituted at any position with alkyl, alkylcarbonyl, benzyl or hydroxyalkyl, or can alternatively form a lactam group with the nitrogen atom of the ring, and, where they exist, their pharmaceutically acceptable salts and optical isomers, are useful as anxiolytics.