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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-(PIPERIDIN-1-YL)PROPANOIC ACID.HCl

CC(C(=O)O)N1CCCCC1.Cl Request for Quotation
Chemical Name: 2-(PIPERIDIN-1-YL)PROPANOIC ACID.HCl
CAS Number: 69181-71-1
Product Number: AG00FD3O(AGN-PC-0WAL6O)
Synonyms:
MDL No:
Molecular Formula: C8H16ClNO2
Molecular Weight: 193.6711

Identification/Properties

Computed Properties
Molecular Weight:
157.213g/mol
XLogP3:
-1.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
157.11g/mol
Monoisotopic Mass:
157.11g/mol
Topological Polar Surface Area:
40.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
141
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(piperidin-1-yl)propanoic acid, also known as piperic acid, is a versatile compound commonly utilized in chemical synthesis. This compound plays a crucial role in organic chemistry as a key intermediate in the synthesis of various pharmaceuticals and fine chemicals. Its unique chemical structure containing a piperidine ring and a carboxylic acid moiety makes it a valuable building block for the preparation of diverse compounds. In chemical synthesis, 2-(piperidin-1-yl)propanoic acid can be used as a precursor for the synthesis of biologically active molecules, such as drugs, agrochemicals, and materials with specific properties.The presence of the piperidine ring in its structure imparts favorable properties to the compounds derived from 2-(piperidin-1-yl)propanoic acid, enhancing their biological activity and pharmacokinetic profiles. Additionally, the carboxylic acid functionality allows for further derivatization through various chemical reactions, expanding the scope of applications in organic synthesis.Overall, the strategic use of 2-(piperidin-1-yl)propanoic acid in chemical synthesis enables the efficient construction of complex molecules with tailored properties for a wide range of industrial and scientific applications.