(4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid

Name: (4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid
Brand: ChemScene
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CAS No. 949023-16-9
Cat. No. CS-0150397
Purity≥98%
MDL No.MFCD11617943

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Excepted Quantity	$0.00
FedEx Limited Quantities Ground	$0.00
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(4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid|CS-0150397

Structure of 949023-16-9

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General Information

CAS No. 949023-16-9
Cat. No. CS-0150397
Purity ≥98%
MDL No. MFCD11617943
Storage 4°C
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₂₄H₂₁NO₅
Molecular Weight 403.43
Synonym(s) Said chain of Paclitaxel 1
SMILES COC1=CC=C(C=C1)C2N([C@@H](C3=CC=CC=C3)[C@H](C(=O)O)O2)C(=O)C4=CC=CC=C4

Description

This oxazolidine derivative features a chiral scaffold with defined (4S,5R) stereochemistry, integrating a benzoyl group at C3, a 4-methoxyphenyl substituent at C2, and a phenyl moiety at C4. The carboxylic acid at C5 enables conjugation or derivatization, supporting its use in asymmetric synthesis and medicinal chemistry applications.

Application

(4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid serves as a stereochemically defined chiral building block for the synthesis of oxazolidinone-containing pharmaceutical intermediates. Its well-defined stereocenters and orthogonal functional groups enable reliable derivatization in peptide coupling and asymmetric synthesis. The molecule exhibits bench stability and facilitates purification via standard chromatographic methods, making it suitable for scalable medicinal chemistry campaigns requiring controlled stereochemistry and functional group compatibility.

Safety Information

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GHS Pictogram :	GHS No : GHS07
Signal Word : Warning	UN#: N/A
Class : N/A	Packing Group : N/A
Hazard Statements : H302-H315-H319-H335
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501

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Computational Chemistry Data

TPSA 76.07
LogP 4.0609
H_Acceptors 4
H_Donors 1
Rotatable_Bonds 5

Other Classifications

Building Blocks Skeleton Aliphatic heterocycle compounds Oxazolidine compounds

Building Blocks Skeleton Aromatic ring compounds Benzene compounds

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Key Words

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(4S,5R)-3-Benzoyl-2-(4-methoxyphenyl)-4-phenyloxazolidine-5-carboxylic acid

CAS No. 949023-16-9

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