857490-18-7

Basic information

• Product Name: (S)-2-(PIPERIDIN-1-YL)PROPANOIC ACID
• Synonyms: (S)-2-(PIPERIDIN-1-YL)PROPANOIC ACID
• CAS NO: 857490-18-7
• Molecular Formula: C8H15NO2
• Molecular Weight: 157.21
• Mol File: 857490-18-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 259.9±23.0 °C(Predicted)
• Appearance: /
• Density: 1.089±0.06 g/cm3(Predicted)
• PKA: 2.56±0.10(Predicted)
• CAS DataBase Reference: (S)-2-(PIPERIDIN-1-YL)PROPANOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(PIPERIDIN-1-YL)PROPANOIC ACID(857490-18-7)
• EPA Substance Registry System: (S)-2-(PIPERIDIN-1-YL)PROPANOIC ACID(857490-18-7)

Safety Data

• Hazardous Substances Data: 857490-18-7(Hazardous Substances Data)

Upstream product

• 111-24-0 1,5-dibromo-pentane 
• 56-41-7 L-alanin 
• 1115-59-9 (S)-alanine ethyl ester hydrochloride 
• 110-89-4 piperidine 
• 127-17-3 2-oxo-propionic acid 
• 63909-12-6 2-piperidino-propionic acid ethyl ester 

Relevant articles and documents

Method for producing amines by homogeneously catalyzed reductive amination of carbonyl compounds

The invention relates to the preparation of chiral or achiral amines by reaction of aldehydes or ketones with ammonia or primary or secondary amines in the presence of hydrogen and in the presence of homogeneous metal catalysts under mild conditions. Metal catalysts which can be used are complexes of late transition metals with chiral or achiral phosphorus-containing ligands.

Diphenylboron Chelates of α-(Dialkylamino)carboxylic Acids and their N-Oxides

α-(Dialkylamino)carboxylic acids and their N-oxides react with oxybis(diphenylborane) or similar diphenylborane derivatives to give five- or six-membered diphenylboron chelate rings, respectively, the structure of which is supported by spectroscopic evidence.