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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)-

3-Piperidineaceticacid, hydrochloride (1:1)

OC(=O)CC1CCCNC1.Cl Request for Quotation
Chemical Name: 3-Piperidineaceticacid, hydrochloride (1:1)
CAS Number: 71985-81-4
Product Number: AG00FA9U(AGN-PC-0IJJON)
Synonyms:
MDL No: MFCD02181158
Molecular Formula: C7H14ClNO2
Molecular Weight: 179.6446

Identification/Properties

Computed Properties
Molecular Weight:
179.644g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
179.071g/mol
Monoisotopic Mass:
179.071g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
125
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:
2
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Piperidin-3-yl)acetic acid hydrochloride is a versatile compound frequently used in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure provides a convenient and efficient method for introducing the piperidine moiety into organic molecules, thereby enabling the synthesis of compounds with diverse biological activities.In chemical synthesis, 2-(Piperidin-3-yl)acetic acid hydrochloride serves as a valuable starting material for the preparation of analogs and derivatives of biologically active compounds, such as neurotransmitters, pharmaceutical drugs, and natural products. By utilizing this compound as a core component, chemists can modify its structure to fine-tune the properties of the resulting molecules, including their potency, selectivity, and pharmacokinetic profiles.Furthermore, the presence of the piperidine functional group in 2-(Piperidin-3-yl)acetic acid hydrochloride offers opportunities for the construction of complex molecular scaffolds through various synthetic transformations, such as substitutions, additions, and cyclizations. This compound's compatibility with a wide range of synthetic methods allows for the efficient synthesis of structurally diverse compounds with potential applications in medicinal chemistry, materials science, and other interdisciplinary fields.Overall, the strategic incorporation of 2-(Piperidin-3-yl)acetic acid hydrochloride in chemical synthesis enables the rapid and cost-effective assembly of novel molecules with tailored properties, making it a valuable tool for researchers and synthetic chemists seeking to develop innovative compounds for various industrial and scientific applications.