320573-07-7

Basic information

• Product Name: 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-8-bromo-1,10-phenanthroline
• Synonyms: 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-8-bromo-1,10-phenanthroline
• CAS NO: 320573-07-7
• Molecular Weight: 555.428
• Mol File: 320573-07-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-8-bromo-1,10-phenanthroline(CAS DataBase Reference)
• NIST Chemistry Reference: 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-8-bromo-1,10-phenanthroline(320573-07-7)
• EPA Substance Registry System: 2,9-bis(2,6-dimethoxyphenyl)-3-ethynyl-8-bromo-1,10-phenanthroline(320573-07-7)

Safety Data

• Hazardous Substances Data: 320573-07-7(Hazardous Substances Data)

Upstream product

• 320573-12-4 2-(2,6-dimethoxyphenyl)-3-trimethylsilylethynyl-8-bromo-1,10-phenanthroline 
• 320573-11-3 2-(2,6-dimethoxyphenyl)-3,8-dibromo-1,10-phenanthroline 
• 16932-45-9 1-bromo-2,6-dimethoxybenzene 
• 320573-13-5 2,9-bis(2,6-dimethoxyphenyl)-3-trimethylsilylethynyl-8-bromo-1,10-phenanthroline 
• 100125-12-0 3,8-dibromo-1,10-phenathroline 

Relevant articles and documents

A highly regioselective Sonogashira coupling as a key step in the preparation of the first phenanthroline with two diverse reactive groups in 3,8-positions

(Matrix presented) The preparation of 3,8-unsymmetric phenanthrolines is described. Desymmetrization of 3,8-dibromophenanthroline was achieved after monoarylation followed by regioselective Pd-catalyzed monoalkynylation that was controlled by the methoxy