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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)-

tert-butyl N-(1-acetylpiperidin-4-yl)carbamate

O=C(OC(C)(C)C)NC1CCN(CC1)C(=O)C Request for Quotation
Chemical Name: tert-butyl N-(1-acetylpiperidin-4-yl)carbamate
CAS Number: 283167-28-2
Product Number: AG00BF7Y(AGN-PC-03U3EP)
Synonyms:
MDL No:
Molecular Formula: C12H22N2O3
Molecular Weight: 242.3147

Identification/Properties

Computed Properties
Molecular Weight:
242.319g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
242.163g/mol
Monoisotopic Mass:
242.163g/mol
Topological Polar Surface Area:
58.6A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
289
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-Butyl (1-acetylpiperidin-4-yl)carbamate is a versatile compound frequently employed in chemical synthesis as a protecting group. This specific derivative serves as a valuable tool in organic chemistry by selectively masking reactive functional groups to facilitate complex transformations. Through the strategic incorporation of tert-Butyl (1-acetylpiperidin-4-yl)carbamate into a synthetic pathway, chemists can effectively shield sensitive moieties from unwanted side reactions or harsh reaction conditions. This protection allows for precise control over the sequence of chemical reactions, enabling the synthesis of intricate molecules with high efficiency and selectivity. In the realm of medicinal chemistry, this compound finds application in the synthesis of pharmaceutical intermediates and bioactive compounds, where the protection of specific functional groups is essential for successful molecular assembly. Furthermore, the tert-Butyl (1-acetylpiperidin-4-yl)carbamate can be selectively removed under mild conditions, revealing the original functional groups and allowing for the subsequent elaboration of the target molecule. This compound's role as a protecting group exemplifies its significance in enabling the synthesis of diverse and structurally complex molecules essential for various scientific and industrial applications.