1268372-68-4

Basic information

• Product Name: (E)-N-(2-(3-hydroxyprop-1-enyl)-4,5-dimethoxyphenethyl)acetamide
• Synonyms: (E)-N-(2-(3-hydroxyprop-1-enyl)-4,5-dimethoxyphenethyl)acetamide
• CAS NO: 1268372-68-4
• Molecular Weight: 279.336
• Mol File: 1268372-68-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (E)-N-(2-(3-hydroxyprop-1-enyl)-4,5-dimethoxyphenethyl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-N-(2-(3-hydroxyprop-1-enyl)-4,5-dimethoxyphenethyl)acetamide(1268372-68-4)
• EPA Substance Registry System: (E)-N-(2-(3-hydroxyprop-1-enyl)-4,5-dimethoxyphenethyl)acetamide(1268372-68-4)

Safety Data

• Hazardous Substances Data: 1268372-68-4(Hazardous Substances Data)

Upstream product

• 66384-45-0 N-acetyl-2-iodo-4,5-dimethoxy-β-phenethylamine 
• 82994-41-0 (E)-3-(tri-n-butylstannyl)-2-propen-1-ol 

Downstream Products

• 1268372-72-0 (E)-3-(2-(2-acetamidoethyl)-4,5-dimethoxyphenyl)allyl methyl carbonate 

Relevant articles and documents

Iridium-catalyzed asymmetric intramolecular allylic amidation: Enantioselective synthesis of chiral tetrahydroisoquinolines and saturated nitrogen heterocycles

For the first time iridium catalysis has been used for the synthesis of chiral tetrahydroisoquinolines with excellent yields and high enantioselectivities (see scheme; cod=1,5-cyclooctadiene, DBU=1,8- diazabicyclo[5.4.0]undec-7-ene). These products are important chiral building blocks for the synthesis of biologically active compounds, in particular alkaloids. Copyright