1314887-12-1

Basic information

• Product Name: (S)-methyl 4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylbutanoate
• Synonyms: (S)-methyl 4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylbutanoate
• CAS NO: 1314887-12-1
• Molecular Weight: 278.348
• Mol File: 1314887-12-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (S)-methyl 4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl 4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylbutanoate(1314887-12-1)
• EPA Substance Registry System: (S)-methyl 4-((S)-2,2-dimethyl-1,3-dioxolan-4-yl)-2-phenylbutanoate(1314887-12-1)

Safety Data

• Hazardous Substances Data: 1314887-12-1(Hazardous Substances Data)

Upstream product

• 103-82-2 phenylacetic acid 
• 67987-67-1 (4S)-4-(2-iodoethyl)-2,2-dimethyl-1,3-dioxolane 
• 18107-18-1 diazomethyl-trimethyl-silane 

Relevant articles and documents

Highly enantioselective direct alkylation of arylacetic acids with chiral lithium amides as traceless auxiliaries

A direct, highly enantioselective alkylation of arylacetic acids via enediolates using a readily available chiral lithium amide as a stereodirecting reagent has been developed. This approach circumvents the traditional attachment and removal of chiral auxiliaries used currently for this type of transformation. The protocol is operationally simple, and the chiral reagent is readily recoverable.