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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)-

1,3-Piperidinedicarboxylic acid, 1-(phenylmethyl) ester

OC(=O)C1CCCN(C1)C(=O)OCc1ccccc1 Request for Quotation
Chemical Name: 1,3-Piperidinedicarboxylic acid, 1-(phenylmethyl) ester
CAS Number: 78190-11-1
Product Number: AG0032FF(AGN-PC-03BK3L)
Synonyms:
MDL No:
Molecular Formula: C14H17NO4
Molecular Weight: 263.2891

Identification/Properties

Properties
MP:
90-94 °C
BP:
443.9°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
263.293g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
263.116g/mol
Monoisotopic Mass:
263.116g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
325
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:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


N-Cbz-Piperidine-3-carboxylic acid, also known as N-Carbobenzyloxy-piperidine-3-carboxylic acid, is a valuable compound widely used in chemical synthesis. This compound is a versatile building block in organic chemistry due to its unique structure and reactivity.One of the key applications of N-Cbz-Piperidine-3-carboxylic acid is its use as a protecting group in peptide synthesis. The Cbz (carbobenzyloxy) group can protect the amine functionality of the piperidine ring, allowing for selective manipulation of other functional groups in the molecule. This protective group can be selectively removed under mild conditions, enabling the synthesis of complex peptides and peptidomimetics.Additionally, N-Cbz-Piperidine-3-carboxylic acid can serve as a precursor in the synthesis of various pharmaceutical intermediates and bioactive compounds. Its versatile reactivity allows for the introduction of diverse functional groups, enabling the construction of structurally diverse molecules with specific biological activities.Overall, N-Cbz-Piperidine-3-carboxylic acid plays a crucial role in chemical synthesis, particularly in the construction of complex molecules such as peptides and pharmaceutical intermediates. Its unique properties make it a valuable tool for organic chemists seeking to design and create novel compounds for various applications.