122993-10-6

Basic information

• Product Name: p-phenylphenacyl ester of laevorotatory o-phenoxyphenylsulfinylacetic acid
• CAS NO: 122993-10-6
• Molecular Weight: 470.546
• Mol File: 122993-10-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: p-phenylphenacyl ester of laevorotatory o-phenoxyphenylsulfinylacetic acid(CAS DataBase Reference)
• NIST Chemistry Reference: p-phenylphenacyl ester of laevorotatory o-phenoxyphenylsulfinylacetic acid(122993-10-6)
• EPA Substance Registry System: p-phenylphenacyl ester of laevorotatory o-phenoxyphenylsulfinylacetic acid(122993-10-6)

Safety Data

• Hazardous Substances Data: 122993-10-6(Hazardous Substances Data)

Upstream product

• 135-73-9 2-Bromo-4'-phenylacetophenone 
• 122993-07-1 o-phenoxyphenylsulfinylacetic acid 
• 55710-19-5 2-phenoxybenzenethiol 
• 107412-83-9 o-phenoxyphenylthioglycolic acid 
• 2688-84-8 2-phenoxyaniline 
• 122993-07-1 laevorotatory o-phenoxyphenylsulfinylacetic acid 

Relevant articles and documents

EFFECT OF MOLECULAR STRUCTURE ON OPTICAL PROPERTIES OF SULFOXIDE SYSTEMS. o-PHENOXYPHENYLSULFINYLACETIC ACIDS AND SOME OF THEIR DERIVATIVES. PART II

The synthesis and principal properties of o-phenoxyphenylthioglycolic as well as o-phenoxyphenylsulfinyl- and sulfonylacetic acids are described.The racemic sulfoxide was resolved by fractional crystallization of its diastereomeric salts with optically active bases.The configurations of the enantiomers were elucidated.Optical rotatory dispersion of the dextro-rotatory enantiomer, its p-bromo and p-phenylphenacyl esters and amide was determined in the region 300 a, ΔS, ΔH) of racemization of dextrorotatory o-phenoxyphenylsulfinylacetic acid were determined by the classical kinetic methods.