1363440-02-1

Basic information

• Product Name: N-(1-(4-iodophenyl)propan-2-yl)acetamide
• Synonyms: N-(1-(4-iodophenyl)propan-2-yl)acetamide
• CAS NO: 1363440-02-1
• Molecular Weight: 289.116
• Mol File: 1363440-02-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: N-(1-(4-iodophenyl)propan-2-yl)acetamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(1-(4-iodophenyl)propan-2-yl)acetamide(1363440-02-1)
• EPA Substance Registry System: N-(1-(4-iodophenyl)propan-2-yl)acetamide(1363440-02-1)

Safety Data

• Hazardous Substances Data: 1363440-02-1(Hazardous Substances Data)

Upstream product

• 25309-64-2 4-ethyl-1-iodobenzene 
• 75-05-8 acetonitrile 
• 92520-16-6 N-(1-(4-bromophenyl)propan-2-yl)acetamide 
• 24358-62-1 1-(4-bromophenyl)ethylamine 

Downstream Products

• 1260955-18-7 (RS)-N-(1-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyl)acetamide 

Relevant articles and documents

A unified photoredox-catalysis strategy for C(sp3)-H hydroxylation and amidation using hypervalent iodine

We report a unified photoredox-catalysis strategy for both hydroxylation and amidation of tertiary and benzylic C-H bonds. Use of hydroxyl perfluorobenziodoxole (PFBl-OH) oxidant is critical for efficient tertiary C-H functionalization, likely due to the enhanced electrophilicity of the benziodoxole radical. Benzylic methylene C-H bonds can be hydroxylated or amidated using unmodified hydroxyl benziodoxole oxidant Bl-OH under similar conditions. An ionic mechanism involving nucleophilic trapping of a carbocation intermediate by H2O or CH3CN cosolvent is presented.

AZETIDINE DERIVATIVES

Azetidine derivatives of which the following is exemplary and their use in the treatment of obesity, diabetes or dyslipidemia.