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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-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid

O=C(N1CC(C(C1)C(=O)O)c1ccccc1)OC(C)(C)C Request for Quotation
Chemical Name: 1-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid
CAS Number: 939757-89-8
Product Number: AG003D4C(AGN-PC-04SL4Y)
Synonyms:
MDL No:
Molecular Formula: C16H21NO4
Molecular Weight: 291.3422

Identification/Properties

Properties
BP:
441.5 °C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
291.347g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
291.147g/mol
Monoisotopic Mass:
291.147g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
396
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The 1-(tert-Butoxycarbonyl)-4-phenylpyrrolidine-3-carboxylic acid is a versatile compound widely used in chemical synthesis for the protection of amine functionalities. Its application extends to the synthesis of diverse organic molecules, particularly in peptide chemistry. By utilizing this compound as a protecting group for amines, chemists can selectively manipulate specific functional groups within a molecule, enabling precise control over the reaction pathways. This compound plays a crucial role in the construction of complex organic molecules and the development of novel pharmaceuticals through strategic chemical synthesis approaches.