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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)-

Carbamic acid, [(3S)-2-oxo-3-piperidinyl]-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)N[C@H]1CCCNC1=O Request for Quotation
Chemical Name: Carbamic acid, [(3S)-2-oxo-3-piperidinyl]-, 1,1-dimethylethyl ester
CAS Number: 92235-39-7
Product Number: AG0032GZ(AGN-PC-0ON57H)
Synonyms:
MDL No: MFCD08166304
Molecular Formula: C10H18N2O3
Molecular Weight: 214.2615

Identification/Properties

Properties
MP:
100 - 101 °C
BP:
405.6 °C at 760 mmHg
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
214.265g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
214.132g/mol
Monoisotopic Mass:
214.132g/mol
Topological Polar Surface Area:
67.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
258
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
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-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(S)-3-(Boc-amino)-2-piperidone is a versatile compound that plays a crucial role in chemical synthesis. This compound is commonly used as a building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. Its unique structure allows for efficient manipulation and modification, making it a valuable tool in the development of new molecules.One key application of (S)-3-(Boc-amino)-2-piperidone is in the synthesis of peptides and peptide derivatives. Peptides are essential components in biological systems and have numerous therapeutic applications. By incorporating (S)-3-(Boc-amino)-2-piperidone into peptide synthesis, chemists can introduce specific functional groups and stereochemistry, enhancing the properties and activities of the resulting peptides.Additionally, (S)-3-(Boc-amino)-2-piperidone can serve as a starting material for the preparation of chiral compounds. Its chirality allows for the creation of enantiomerically pure substances, which is crucial in the development of pharmaceuticals with defined biological activities.Furthermore, this compound can be utilized in the production of heterocyclic compounds, which are prevalent in many drug molecules and bioactive compounds. (S)-3-(Boc-amino)-2-piperidone's structural versatility enables chemists to access a diverse array of heterocycles, expanding the scope of chemical synthesis and drug discovery.Overall, (S)-3-(Boc-amino)-2-piperidone is a valuable component in chemical synthesis, offering opportunities for the design and creation of complex molecules with important applications in various industries.