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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, [1-(phenylmethyl)-4-piperidinyl]-, 1,1-dimethylethyl ester

O=C(OC(C)(C)C)NC1CCN(CC1)Cc1ccccc1 Request for Quotation
Chemical Name: Carbamic acid, [1-(phenylmethyl)-4-piperidinyl]-, 1,1-dimethylethyl ester
CAS Number: 73889-19-7
Product Number: AG003DZU(AGN-PC-0LB4QR)
Synonyms:
MDL No: MFCD03093979
Molecular Formula: C17H26N2O2
Molecular Weight: 290.4005

Identification/Properties

Properties
MP:
122-125 °C
BP:
400.9 °C at 760 mmHg
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
290.407g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
290.199g/mol
Monoisotopic Mass:
290.199g/mol
Topological Polar Surface Area:
41.6A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
324
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


1-Benzyl-4-(tert-butoxycarbonylamino)piperidine, also known as $name$, is a valuable compound widely used in chemical synthesis. It serves as a versatile building block in the preparation of various pharmaceuticals and fine chemicals. The presence of the benzyl group provides stability and rigidity to the molecule, making it an ideal precursor in organic reactions. Additionally, the tert-butoxycarbonyl (Boc) protecting group offers protection for the primary amine functionality, allowing for selective transformations and ensuring high yields in multi-step syntheses. $name$ is commonly utilized in the synthesis of complex molecules, such as natural products and drug candidates, owing to its structural features that enable facile modification and manipulation. Its application extends to the preparation of bioactive compounds, agrochemicals, and materials with tailored properties, highlighting its significance in contemporary synthetic chemistry.