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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)-

1-[(2-methylpropan-2-yl)oxycarbonyl]-4-phenylpiperidine-2-carboxylic acid

[O-]C(=O)C1CC(CCN1C(=O)OC(C)(C)C)c1ccccc1 Request for Quotation
Chemical Name: 1-[(2-methylpropan-2-yl)oxycarbonyl]-4-phenylpiperidine-2-carboxylic acid
CAS Number: 261777-31-5
Product Number: AG002S2V(AGN-PC-07A818)
Synonyms:
MDL No:
Molecular Formula: C17H22NO4-
Molecular Weight: 304.3609

Identification/Properties

Computed Properties
Molecular Weight:
305.374g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
305.163g/mol
Monoisotopic Mass:
305.163g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
22
Formal Charge:
0
Complexity:
409
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
2
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


The 1-(tert-Butoxycarbonyl)-4-phenylpiperidine-2-carboxylic acid is a versatile chemical compound widely utilized in chemical synthesis processes. In organic synthesis, it serves as a key building block for the construction of complex molecules due to its unique structural properties. This compound is commonly employed as a protecting group for amines, providing a temporary shield for amine functional groups during reactions. By introducing the 1-(tert-Butoxycarbonyl)-4-phenylpiperidine-2-carboxylic acid as a protecting group, chemists can selectively modify other reactive sites on a molecule without affecting the amine functionality. This strategic use facilitates the synthesis of intricate organic compounds with specific structural arrangements and functionalities required for various applications in the fields of pharmaceuticals, materials science, and agrochemicals. The versatility of 1-(tert-Butoxycarbonyl)-4-phenylpiperidine-2-carboxylic acid in chemical synthesis highlights its significance as a valuable tool for designing and constructing diverse molecular architectures.