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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)-

4-Piperidinecarboxylic acid, 1-acetyl-

OC(=O)C1CCN(CC1)C(=O)C Request for Quotation
Chemical Name: 4-Piperidinecarboxylic acid, 1-acetyl-
CAS Number: 25503-90-6
Product Number: AG003DWM(AGN-PC-0JLL4F)
Synonyms:
MDL No:
Molecular Formula: C8H13NO3
Molecular Weight: 171.1937

Identification/Properties

Properties
MP:
180-184 °C(lit.)
BP:
374°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.4750 (estimate)
Computed Properties
Molecular Weight:
171.196g/mol
XLogP3:
-0.3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
171.09g/mol
Monoisotopic Mass:
171.09g/mol
Topological Polar Surface Area:
57.6A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
195
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H317-H319-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


1-Acetyl-4-Piperidinecarboxylic Acid, also known as APAC, is a versatile chemical compound widely used in chemical synthesis. This organic compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, 1-Acetyl-4-Piperidinecarboxylic Acid serves as a key building block for the synthesis of complex organic molecules. Its piperidine ring provides a stable and versatile scaffold, allowing for the introduction of different functional groups through various chemical reactions. This enables chemists to modify the molecular structure of compounds, leading to the development of new drugs, pesticides, and other valuable products.Moreover, the acetyl group attached to the piperidine ring enhances the compound's solubility and stability, making it easier to handle and manipulate in laboratory settings. The presence of the carboxylic acid functional group further expands the compound's utility by offering opportunities for derivatization and cross-coupling reactions.Overall, 1-Acetyl-4-Piperidinecarboxylic Acid is a valuable tool in chemical synthesis, enabling chemists to access diverse chemical space and create novel molecules with desired properties for various applications.