14788-14-8

Basic information

• Product Name: 1-pyrrolidinepropanoic acid(HCl)
• Synonyms: 1-pyrrolidinepropanoic acid(HCl);3-Pyrrolidin-1-yl-propionic acid hydrochloride ,98%;1-Pyrrolidinepropanoic acid, hydrochloride;3-PYRROLIDIN-1-YL-PROPIONIC ACID HCL(RS20013275)
• CAS NO: 14788-14-8
• Molecular Formula: C7H13NO2·HCl
• Molecular Weight: 0
• Mol File: 14788-14-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-pyrrolidinepropanoic acid(HCl)(CAS DataBase Reference)
• NIST Chemistry Reference: 1-pyrrolidinepropanoic acid(HCl)(14788-14-8)
• EPA Substance Registry System: 1-pyrrolidinepropanoic acid(HCl)(14788-14-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 14788-14-8(Hazardous Substances Data)

Usage

Chemical Properties

White solid

Upstream product

• 478407-83-9 tert-butyl 3-(pyrrolidin-1-yl)propanoate 
• 6317-35-7 ethyl 3-tetrahydro-1H-1-pyrrolilpropanoate 

Relevant articles and documents

Synthesis, IR and NMR studies of zwitterionic ω-(1-pyrrolidine)alkanocarboxylic acids and their N-methyl derivatives

Six ω-(1-pyrrolidine)alkanocarboxylic acid hydrohalides [C4H8N+H(CH2)(n)COOH · X-] and 1-(ω-carboxyalkyl)-1-methyl-pyrrolidinium hydrohalides [C4H8N+CH3(CH2)(n)COOH · X- (n = 1,2,3,4,5,10)] and their sodium and inner salts were synthesized, respectively. IR, 1H and 13C NMR spectra were analyzed with regard to the increasing distance effect on the interaction between the positive nitrogen atom with the negative carboxylic group. The configuration of the pyrrolidine ring was also discussed.

N-heterocyclic propylidene-1,1-bisphosphonic acids, their production and a pharmaceutical composition

The present invention relates to compounds of formula in which R1 -R8 can be the same or different and stand for hydrogen or a straight or branched aliphatic C1 -C10 hydrocarbon radical. In addition, R3 when taken together with either R1 or R5 can form a saturated aliphatic 5-, 6-or 7-membered ring, which may be substituted with one or more C1 -C4 -alkyl radicals. The present compounds are effective e.g. in drugs influencing calcium metabolism.