ChemicalBook Product Catalog Pharmaceutical intermediates Heterocyclic compound Pyridine compound Pyridine derivatives 1-Acetyl-4-piperidinecarboxylic acid

1-Acetyl-4-piperidinecarboxylic acid

1-Acetyl-4-piperidinecarboxylic acid Basic information
Product Name:1-Acetyl-4-piperidinecarboxylic acid
Synonyms:4-Piperidinecarboxylic acid, 1-acetyl-;RARECHEM AL BO 0864;N-ACETYLISONIPECOTIC ACID;TIMTEC-BB SBB000171;1-Acetylpiperidine-4-CarboxylicAcid/N-AcetylisonipecoticAcid;1-Acetylpiperidine-4-carboxylic acid, 95+%;1-Acetyl-4-piperidine;ac-dl-inp-oh
CAS:25503-90-6
MF:C8H13NO3
MW:171.19
EINECS:247-049-6
Product Categories:Building Blocks;C8;Heterocycles;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines;Piperidines, Piperidones, Piperazines;Pyridine series;PiperidineDerivative;API intermediates;Heterocyclic Compounds;Neurochemicals;Carboxylic Acids;Pyrans, Piperidines & Piperazines
Mol File:25503-90-6.mol
1-Acetyl-4-piperidinecarboxylic acid Structure
1-Acetyl-4-piperidinecarboxylic acid Chemical Properties
Melting point 180-184 °C (lit.)
Boiling point 301.17°C (rough estimate)
density 1.1998 (rough estimate)
refractive index 1.4750 (estimate)
storage temp. Sealed in dry,Room Temperature
solubility Methanol (Slightly), Water (Slightly)
pka4.35±0.20(Predicted)
form Crystalline Powder
color White to beige
Water Solubility 50 g/L (20 ºC)
BRN 389577
CAS DataBase Reference25503-90-6(CAS DataBase Reference)
NIST Chemistry Reference1-Acetyl-4-piperidinecarboxylic acid(25503-90-6)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-43
Safety Statements 26-36-37/39
WGK Germany 2
HazardClass IRRITANT
HS Code 29339900
MSDS Information
ProviderLanguage
1-Acetylpiperidine-4-carboxylic acid English
SigmaAldrich English
ACROS English
ALFA English
1-Acetyl-4-piperidinecarboxylic acid Usage And Synthesis
Chemical PropertiesWhite Crystalline Solid
UsesA synthetic intermediate in the preparation of CNS depressants
UsesReactant for synthesis of:• ;Triazole derivatives1• ;Antiproliferative agents2• ;CDK inhibitors3• ;CCR5 antagonists for HIV treatment4• ;nhNK1 antagonists5• ;Piperidine derivatives6
UsesMetabolite fingerprinting in transgenic Nicotiana tabacum altered by the Escherichia coli glutamate dehydrogenase gene.
1-PROPIONYL-4-PIPERIDINECARBOXYLIC ACID 1-BENZOYLPIPERIDINE-4-CARBOXYLIC ACID ETHYL 1-(4-CHLORO-3-NITROBENZOYL)PIPERIDINE-4-CARBOXYLATE N-ACETYL-L-TYROSINE ETHYL ESTER METHYL 1-(3-NITROBENZOYL)-4-PIPERIDINECARBOXYLATE ETHYL 1-(2-CHLOROACETYL)-4-PIPERIDINECARBOXYLATE Acetylacetone AURORA 426 Acetylferrocene tributyl acetocitrate ethyl 1-(pyrrolidin-2-ylcarbonyl)piperidine-4-carboxylate 1-(PYRIDIN-3-YLCARBONYL)PIPERIDINE-4-CARBOXYLIC ACID Acetyl chloride ETHYL 1-(4-CHLOROBENZOYL)-4-PIPERIDINECARBOXYLATE Isonipecotic acid CARBOXYLIC ACID 1-(4-nitrobenzoyl)piperidine-4-carboxylic acid 1-Acetyl-4-piperidinecarboxylic acid
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