CAS 89662-51-1

benzyl (4S)-5-oxo-4-(3-oxobutyl)oxazolidine-3-carboxylate

Description:

Benzyl (4S)-5-oxo-4-(3-oxobutyl)oxazolidine-3-carboxylate is a chemical compound characterized by its oxazolidine ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen atoms. This substance features a carboxylate group, contributing to its acidic properties, and a benzyl group that enhances its lipophilicity, potentially affecting its solubility and reactivity. The presence of a ketone functional group (5-oxo) and an additional carbon chain (3-oxobutyl) suggests that it may participate in various chemical reactions, such as nucleophilic attacks or condensation reactions. The stereochemistry indicated by the (4S) designation implies specific spatial arrangements of atoms, which can influence the compound's biological activity and interactions. Overall, this compound may be of interest in pharmaceutical chemistry, particularly in the development of drugs or intermediates due to its unique structural features and potential reactivity.

Formula: C₁₅H₁₇NO₅

InChI: InChI=1/C15H17NO5/c1-11(17)7-8-13-14(18)21-10-16(13)15(19)20-9-12-5-3-2-4-6-12/h2-6,13H,7-10H2,1H3/t13-/m0/s1

SMILES: CC(=O)CC[C@H]1C(=O)OCN1C(=O)OCc1ccccc1

Synonyms:

• (4S)-5-Oxo-4-(3-oxobutyl)-3-oxazolidinecarboxylic Acid PhenylMethyl Ester
• (S)-3-BENZYLOXYCARBONYL-4-(3-OXOBUTYL)-5-OXAZILIDINONE

(S)-3-Benzyloxycarbonyl-4-(3-oxobutyl)-5-oxazilidinone

Controlled Product

CAS: 89662-51-1

Applications (S)-3-Benzyloxycarbonyl-4-(3-oxobutyl)-5-oxazilidinone (cas# 89662-51-1) is a compound useful in organic synthesis.
References Wallen, E., et al.: Bioorg. Med. Chem., 11, 3611 (2003),

Formula: C₁₅H₁₇NO₅

Color and Shape: Neat

Molecular weight: 291.30

Ref: TR-B285920