1426835-58-6

Basic information

• Product Name: C₃₆H₃₆N₈OSSi
• Synonyms: C₃₆H₃₆N₈OSSi
• CAS NO: 1426835-58-6
• Molecular Weight: 656.886
• Mol File: 1426835-58-6.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: C₃₆H₃₆N₈OSSi(CAS DataBase Reference)
• NIST Chemistry Reference: C₃₆H₃₆N₈OSSi(1426835-58-6)
• EPA Substance Registry System: C₃₆H₃₆N₈OSSi(1426835-58-6)

Safety Data

• Hazardous Substances Data: 1426835-58-6(Hazardous Substances Data)

Upstream product

• 225378-53-0 2-(2-(tert-butyl)-6-methyl-4H-pyran-4-ylidene)malononitrile 
• 1307899-00-8 4-((2-azidoethyl)(methyl)amino)benzaldehyde 
• 1201-91-8 4-(N-methyl-N-hydroxyethylamino)benzaldehyde 
• 480998-11-6 4,7-bis[(trimethylsilyl)ethynyl]benzo[c][1,2,5]thiadiazole 
• 531512-24-0 C₁₁H₁₅NO₄S 

Relevant articles and documents

Fluorescent dyad for cooperative recognition of copper cation and halogen anion

TMS-ethynyl triazolyl benzothiadiazole (BTD) derivatives have been successfully synthesized by mono deprotection of di-TMS-ethynyl BTD followed by click chemistry. The fluorescence intensity of TMS-ethynyl triazolyl BTD-DCM dyad 8, as well as triazolyl BTD 3, and the DCM derivative 7 could be selectively quenched by Cu2+, but almost not affected by different tested anions. Interestingly, the fluorescence emission of DCM-based fluorophores 7 and 8 was highly sensitive to a combination of Cu2+, F-, or Br- in a sequence dependent manner. With the dyad 8, the detection limit as low as 0.13 ppb could be attained for F- in MeCN. The Cu2+-promoted aerobic oxidative dimerization of DCM moiety to tetrahydrofuran derivatives has also been demonstrated for the first time.