Home Carboxys Piperidine-4-carboxylic acid

Piperidine-4-carboxylic acid

CAS No.:
498-94-2
Catalog Number:
AG00351Y
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
95%
In Stock USA
United States
$13
- +
25g
98%
In Stock USA
United States
$19
- +
100g
98%
In Stock USA
United States
$50
- +
500g
98%
In Stock USA
United States
$188
- +
Product Description
Catalog Number:
AG00351Y
Chemical Name:
Piperidine-4-carboxylic acid
CAS Number:
498-94-2
Molecular Formula:
C6H11NO2
Molecular Weight:
129.1570
MDL Number:
MFCD00006004
IUPAC Name:
piperidine-4-carboxylic acid
InChI:
InChI=1S/C6H11NO2/c8-6(9)5-1-3-7-4-2-5/h5,7H,1-4H2,(H,8,9)
InChI Key:
SRJOCJYGOFTFLH-UHFFFAOYSA-N
SMILES:
OC(=O)C1CCNCC1
EC Number:
207-872-3
UNII:
M5TZP1RWIE
NSC Number:
61049
Properties
Complexity:
108  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
129.079g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
129.159g/mol
Monoisotopic Mass:
129.079g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
49.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-3  
Literature
Title Journal
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Temperature effects on the hydrogen-bond patterns in 4-piperidinecarboxylic acid. Acta crystallographica. Section B, Structural science 20050201
Characterization and crystal structure of cadmium(II) halide complexes with amino acids and their derivatives VI. The comparison of crystal structures of cadmium(II) halide complexes with three kinds of piperidine carboxylic acids. Journal of inorganic biochemistry 20041201
Facile synthesis of 4-substituted-4-aminopiperidine derivatives, the key building block of piperazine-based CCR5 antagonists. Bioorganic & medicinal chemistry letters 20040716
Activation of single heteromeric GABA(A) receptor ion channels by full and partial agonists. The Journal of physiology 20040601
Design, synthesis and anticonvulsive activity of analogs of gamma-vinyl GABA. Farmaco (Societa chimica italiana : 1989) 20040501
Synthetic methodology utilized to prepare substituted imidazole p38 MAP kinase inhibitors. Current opinion in drug discovery & development 20031101
Design, synthesis and anticonvulsive activities of potential prodrugs linked by two-carbon chain. Archives of pharmacal research 20031001
Highly water-soluble derivatives of the anesthetic agent propofol: in vitro and in vivo evaluation of cyclic amino acid esters. European journal of pharmaceutical sciences : official journal of the European Federation for Pharmaceutical Sciences 20030901
Phosphinic, phosphonic and seleninic acid bioisosteres of isonipecotic acid as novel and selective GABA(C) receptor antagonists. Neurochemistry international 20030601
Xanthamide fluorescent dyes. Analytical chemistry 20021215
Sustained ER Ca2+ depletion suppresses protein synthesis and induces activation-enhanced cell death in mast cells. The Journal of biological chemistry 20020419
Zwitterionic 4-piperidinecarboxylic acid monohydrate. Acta crystallographica. Section C, Crystal structure communications 20010801
Short, solubilized polyalanines are conformational chameleons: exceptionally helical if N- and C-capped with helix stabilizers, weakly to moderately helical if capped with rigid spacers. Biochemistry 20010116
Alternative splicing of a Drosophila GABA receptor subunit gene identifies determinants of agonist potency. Neuroscience 20010101
Properties