This compound is a chiral oxazolidine derivative featuring a benzoyl-protected nitrogen, gem-dimethyl substitution, an aryl (phenyl) group, and a carboxylic acid functional group. The defined (4S,5R) stereochemistry makes it a stereochemically controlled synthetic building block. The oxazolidine ring system is widely used in asymmetric and chiral synthesis as a temporary scaffold to control configuration during multistep reactions. The benzoyl group functions as a protecting group for nitrogen, while the rigid ring structure helps maintain stereochemical integrity during downstream transformations. The directory classifies it as a under development API with a synthetic source/manufacturing origin. Other names for this substance include trans-3-Benzoyl-2, 2-dimethyl-4-phenyloxazolidine-5-carboxylic acid, 5-Oxazolidinecarboxylic acid, 3-benzoyl-2, 2-dimethyl-4-phenyl-, (4S and 5R)-. It is also listed for alternate use as: API Intermediate. Its PubChem CID is 10131335.
(4s,5r)-3-Benzoyl-2,2-dimethyl-4-phenyloxazolidine-5-carboxylic acid
| CAS No | 153652-70-1 |
|---|---|
| Molecular Formula | C19H19NO4 |
| Molecular Weight | 325.4 g/mol |
| Synonyms | (4S,5R)-3-benzoyl-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-carboxylic acid |
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Frequently Asked Questions
This compound is a chiral oxazolidine derivative featuring a benzoyl-protected nitrogen, gem-dimethyl substitution, an aryl (phenyl) group, and a carboxylic acid functional group.
The listed CAS number is 153652-70-1.
The listed molecular formula is C19H19NO4.
The listed molecular weight is 325.4 g/mol.
(4S,5R)-3-benzoyl-2,2-dimethyl-4-phenyl-1,3-oxazolidine-5-carboxylic acid.
The source lists trans-3-Benzoyl-2, 2-dimethyl-4-phenyloxazolidine-5-carboxylic acid, 5-Oxazolidinecarboxylic acid, 3-benzoyl-2, 2-dimethyl-4-phenyl-, (4S and 5R)-.