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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]-5-phenylpyrrolidine-3-carboxylic acid

OC(=O)C1CN(C(C1)c1ccccc1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-[(2-methylpropan-2-yl)oxycarbonyl]-5-phenylpyrrolidine-3-carboxylic acid
CAS Number: 885277-76-9
Product Number: AG0047B4(AGN-PC-07YKCU)
Synonyms:
MDL No:
Molecular Formula: C16H21NO4
Molecular Weight: 291.3422

Identification/Properties

Properties
BP:
441.471°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-Boc-5-Phenylpyrrolidine-3-carboxylic acid, also known as Boc-protected phenylpyrrolidine-3-carboxylic acid, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the synthesis of various pharmaceuticals and organic molecules.In chemical synthesis, 1-Boc-5-Phenylpyrrolidine-3-carboxylic acid can be utilized as a key intermediate for the preparation of complex organic compounds. Its Boc (tert-butoxycarbonyl) protecting group provides stability to the molecule during various reaction conditions, allowing for selective functionalization at specific sites.This compound's structural features make it valuable in the construction of heterocyclic frameworks and peptide derivatives. By incorporating 1-Boc-5-Phenylpyrrolidine-3-carboxylic acid into synthetic schemes, chemists can access a wide range of structurally diverse molecules with potential biological activities.Furthermore, the presence of the phenyl and pyrrolidine moieties in this compound imparts unique properties that can influence the pharmacological profile of the final products. Through strategic manipulation of these structural elements, chemists can tailor the properties of the synthesized compounds for desired applications in drug discovery or material science.Overall, the utilization of 1-Boc-5-Phenylpyrrolidine-3-carboxylic acid in chemical synthesis enables efficient access to complex molecules with diverse functionalities, making it a valuable tool for organic chemists working in the field of medicinal chemistry and drug development.