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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-Pyrrolidinecarboxylicacid, 4-hydroxy-2-(hydroxymethyl)-, phenylmethyl ester, (2S,4S)-

OC[C@@H]1C[C@@H](CN1C(=O)OCc1ccccc1)O Request for Quotation
Chemical Name: 1-Pyrrolidinecarboxylicacid, 4-hydroxy-2-(hydroxymethyl)-, phenylmethyl ester, (2S,4S)-
CAS Number: 942308-58-9
Product Number: AG005SAI(AGN-PC-0W3UWP)
Synonyms:
MDL No:
Molecular Formula: C13H17NO4
Molecular Weight: 251.2784

Identification/Properties

Properties
BP:
433.897°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid

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


(2S,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate, also known as $name$, is a valuable compound in chemical synthesis due to its unique structural features and versatile reactivity. This compound is commonly used as a chiral building block in organic synthesis, particularly in the production of pharmaceuticals, fine chemicals, and advanced materials.One key application of (2S,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate is in asymmetric synthesis, where its chiral nature allows for the creation of enantiomerically pure compounds. By incorporating this compound into synthetic pathways, chemists can efficiently access enantiomerically enriched molecules with high stereochemical control. This is essential in drug discovery and development, as many pharmaceuticals require specific stereochemistry to exhibit the desired biological activity.Additionally, (2S,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate can serve as a protecting group for sensitive functional groups during chemical transformations. Its hydroxyl and carboxylic acid moieties can be selectively modified and then readily deprotected to reveal the original functional groups, enabling complex molecule synthesis in a stepwise fashion.Overall, the application of (2S,4S)-Benzyl 4-hydroxy-2-(hydroxymethyl)pyrrolidine-1-carboxylate in chemical synthesis offers chemists a powerful tool for accessing challenging chiral molecules and elaborating complex chemical structures with precision and efficiency.