107022-88-8

Basic information

• Product Name: (R)-3-(hydroxymethyl)-N-((((S)))-1-phenylethyl)pent-4-enamide
• Synonyms: (R)-3-(hydroxymethyl)-N-((((S)))-1-phenylethyl)pent-4-enamide
• CAS NO: 107022-88-8
• Molecular Weight: 233.31
• Mol File: 107022-88-8.mol

Chemical Properties

• CAS DataBase Reference: (R)-3-(hydroxymethyl)-N-((((S)))-1-phenylethyl)pent-4-enamide(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-3-(hydroxymethyl)-N-((((S)))-1-phenylethyl)pent-4-enamide(107022-88-8)
• EPA Substance Registry System: (R)-3-(hydroxymethyl)-N-((((S)))-1-phenylethyl)pent-4-enamide(107022-88-8)

Safety Data

• Hazardous Substances Data: 107022-88-8(Hazardous Substances Data)

Upstream product

• 53627-36-4 3-vinylbutyrolactone 
• 2627-86-3 (S)-1-phenyl-ethylamine 

Downstream Products

• 121959-61-3 (R)-(-)-β-vinyl-γ-butyrolactone 

Relevant articles and documents

Improved Synthesis of Racemate and Enantiomers of Taniguchi Lactone and Conversion of Their C-C Double Bonds into Triple Bonds

cis -2-Butene-1,4-diol was heated with triethyl orthoacetate and p -hydroquinone as catalyst at 170 °C to give racemic Taniguchi lactone. It was converted into diastereomeric amides with (S)-1-phenylethylamine for stereoisomer resolution. The double bonds

Facile production scale synthesis of (S)-Taniguchi lactone: A precious building-block

A cost-efficient and facile synthesis of (S)-4-vinyldihydrofuran-2(3H)-one ((S)-1), better known as (S)-Taniguchi lactone, is described. Racemic Taniguchi lactone rac-1 was ring-opened with (S)-1-benzylmethylamine providing a diastereomeric mixture of hyd

Synthesis and Absolute Configuration of the Acetalic Lignan(+)-Phrymarolin I

The natural (+)-phrymarolin I was stereoselectively synthesized and its absolute configuration was unequivocally determined as being (1S,2S,5R,6S)-1-acetoxy-2-(2-methoxy-4,5-methylenedioxyphenoxy)-6-(2-methoxy-4,5-methylenedioxyphenyl)-3,7-dioxabicyclooctane.

Synthesis and Absolute Configuration of (+)-Phrymarolin I, a Lignan

(+)-Phrymarolin I was synthesized from (S)-(+)-β-vinyl-γ-butyrolactone, and the absolute configuration of the natural product was established as (1S,2S,5R,6R).