1351791-42-8

Basic information

• Product Name: (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalic acid
• Synonyms: (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalic acid
• CAS NO: 1351791-42-8
• Molecular Weight: 341.32
• Mol File: 1351791-42-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalic acid(1351791-42-8)
• EPA Substance Registry System: (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalic acid(1351791-42-8)

Safety Data

• Hazardous Substances Data: 1351791-42-8(Hazardous Substances Data)

Upstream product

• 586-35-6 2-bromo-1,4-benzenedicarboxylic acid 
• 18643-86-2 dimethyl 2-bromoterephthalate 
• 1351791-44-0 dimethyl (S)-2-(4-benzyl-2-oxooxazolidin-3-yl)terephthalate 

Relevant articles and documents

Application of a chiral metal-organic framework in enantioselective separation

A modular approach for the synthesis of highly ordered porous and chiral auxiliary (Evans auxiliary) decorated metal-organic frameworks is developed. Our synthesis strategy, which uses known porous structures as model materials for incorporation of chirality via linker modification, can provide access to a wide range of porous materials suitable for enantioselective separation and catalysis. Chiral analogues of UMCM-1 have been synthesized and investigated for the enantioseparation of chiral compounds in the liquid phase and first promising results are reported. The Royal Society of Chemistry 2011.