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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-Amino-2-piperidinone trifluoroacetate

OC(=O)C(F)(F)F.NC1CCNC(=O)C1 Request for Quotation
Chemical Name: 4-Amino-2-piperidinone trifluoroacetate
CAS Number: 1523618-06-5
Product Number: AG00360X(AGN-PC-0WAKL6)
Synonyms:
MDL No:
Molecular Formula: C7H11F3N2O3
Molecular Weight: 228.1690

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
228.171g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
0
Exact Mass:
228.072g/mol
Monoisotopic Mass:
228.072g/mol
Topological Polar Surface Area:
92.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
186
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
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 4-aminopiperidin-2-one 2,2,2-trifluoroacetate salt is a versatile compound commonly used in chemical synthesis due to its unique properties and high reactivity. This salt serves as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and specialty chemicals. Its trifluoroacetate group enhances the nucleophilicity and stability of the molecule, making it a valuable intermediate in organic transformations.In chemical synthesis, this compound is particularly valuable for introducing the 4-aminopiperidin-2-one moiety into complex molecules. The presence of the trifluoroacetate salt provides a convenient handle for further derivatization, allowing for the incorporation of diverse functional groups or modifications. This versatility makes it an essential reagent in the preparation of bioactive compounds and drug candidates.Additionally, the 4-aminopiperidin-2-one 2,2,2-trifluoroacetate salt can facilitate the formation of key structural motifs in medicinal chemistry, such as heterocycles and amine derivatives. Its reactivity under various reaction conditions enables chemists to access a wide range of molecular scaffolds with high efficiency and selectivity. Overall, this compound plays a crucial role in advancing the field of chemical synthesis and accelerating the discovery of novel compounds with potential therapeutic applications.