171087-98-2

Basic information

• Product Name: [2-(2,3-dimethoxyphenyl)ethynyl]trimethylsilane
• Synonyms: [2-(2,3-dimethoxyphenyl)ethynyl]trimethylsilane
• CAS NO: 171087-98-2
• Molecular Weight: 234.37
• Mol File: 171087-98-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: [2-(2,3-dimethoxyphenyl)ethynyl]trimethylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: [2-(2,3-dimethoxyphenyl)ethynyl]trimethylsilane(171087-98-2)
• EPA Substance Registry System: [2-(2,3-dimethoxyphenyl)ethynyl]trimethylsilane(171087-98-2)

Safety Data

• Hazardous Substances Data: 171087-98-2(Hazardous Substances Data)

Upstream product

• 91-16-7 1,2-dimethoxybenzene 
• 25245-33-4 1-iodo-2,3-dimethoxybenzene 
• 1066-54-2 trimethylsilylacetylene 
• 5424-43-1 3-bromoveratrole 

Downstream Products

• 175844-61-8 1,4-bis(2,3-dimethoxyphenylethynyl)-2,3-dimethoxybenzene 
• 175844-62-9 1,4-bis[2-(2,3-dimethoxyphenyl)ethyl]-2,3-dimethoxybenzene 
• 175844-53-8 1,4-bis<2-(2,3-dihydroxyphenyl)ethyl>-2,3-dihydroxybenzene 
• 175844-60-7 1,4-bis(2,3-dimethoxyphenyl)butane 
• 175844-52-7 1,4-bis(2,3-dihydroxyphenyl)butane 
• 171087-99-3 1-ethynyl-2,3-dimethoxybenzene 
• 171088-00-9 1,3-bis(2,3-dimethoxyphenyl)propyne 
• 171088-01-0 1,3-bis(2,3-dimethoxyphenyl)propane 
• 171088-06-5 3,3'-propane-1,3-diylbis(1,2-benzenediol) 

Relevant articles and documents

Synthesis of bis(catechol) ligands derived from Troeger's base and their dinuclear triple-stranded complexes with titanium(IV) ions

Bis(catechol) ligands derived from 2,8-disubstituted analogues of Troeger's base and monofunctionalized MOM-protected or unprotected catechols bearing both rigid and flexible spacers were synthesized, which gave rise to dissymmetric oxygen donor ligands w

Synthesis of linear oligo(catechol) ligands for the metal directed self-assembling of helicates

The synthesis of the oligo(catechol) systems 1-4 with different substituents, length of the connecting spacer, and number of catechol units is achieved by the use of various coupling reactions (e.g. Wurtz, Glaser-Eglinton, Stephens-Castro). In order to do this methods of preparing the building blocks, 2,3-dimethoxybenzyl bromides 5, 2,3-dimethoxyphenylacetylene (17), or 1,4-dibromo-2,3-dimethoxybenzene (23) have been developed starting with simple catechol (benzene-1,2-diol) derivatives.