137937-89-4

Basic information

• Product Name: Stannane, tributyl(5-phenyl-2-thienyl)-
• CAS NO: 137937-89-4
• Molecular Formula: C22H34SSn
• Molecular Weight: 449.288
• Mol File: 137937-89-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Stannane, tributyl(5-phenyl-2-thienyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Stannane, tributyl(5-phenyl-2-thienyl)-(137937-89-4)
• EPA Substance Registry System: Stannane, tributyl(5-phenyl-2-thienyl)-(137937-89-4)

Safety Data

• Hazardous Substances Data: 137937-89-4(Hazardous Substances Data)

Upstream product

• 825-55-8 2-phenylthiophene 
• 29488-24-2 2-Bromo-5-phenyl-thiophene 
• 1461-22-9 tributyltin chloride 

Downstream Products

• 380626-58-4 1,4-dibutoxy-2,5-di(5'-phenyl-5''-di-2',2''-thienyl)benzene 
• 1428418-21-6 4,7-bis(5-phenylthiophen-2-yl)-2-(pyridin-4-yl)-2H-benzo[d][1,2,3]triazole 
• 94331-55-2 1-methyl-2-(5-phenylthiophen-2-yl)-1H-benzo[d]imidazole 
• 1391086-22-8 3,7-bis(dodecylthio)-2,6-(5-phenyl-2-thienyl)benzo[1,2-b;4,5-b']dithiophene 
• 1311100-10-3 C₅₄H₆₆S₄ 
• 1263302-44-8 2,6-bis(thiophene-2'-yl)-9,10-bis(triisopropylsilylethynyl)anthracene 
• 1160124-23-1 2,5-bis(5-phenyl-2-thienyl)terephthalaldehyde 
• 137937-80-5 4-Amino-5-(5-phenyl-thiophen-2-yl)-pyrimidin-2-ol 
• 887256-75-9 4'-(2,5-dimethoxyphenyl)-5,5'''-diphenyl-2,2':5',2'':5'',2'''-quaterthiophene 
• 450358-66-4 {2-[bis(carboxymethyl)amino]-5-(5-phenylthiophen-2-yl)phenoxy}acetic acid trimethyl ester 
• 83495-30-1 5,5′-diphenyl-2,2′-bithiophene 
• 143324-59-8 [5-(5-Phenyl-thiophen-2-yl)-2-trimethylsilanyloxy-pyrimidin-4-yl]-trimethylsilanyl-amine 

Relevant articles and documents

With long-wave absorption characteristic of a series of 2, 3, 5, 6-tetrahydro-thiophene substituted BODIPY dye and method for preparing same

The invention relates to a series of 2,3,5,6-quaterthiophene substituted BODIPY (boron dipyrromethene) dyes with long wave absorption characteristics and a preparation method of the 2,3,5,6-quaterthiophene substituted BODIPY dyes. The preparation method c

Comprehensive analysis of fragment orbital interactions to build highly π-conjugated thienylene-substituted phenylene oligomers

π-Conjugated thienylene-phenylene oligomers with fluorinated and dialkoxylated phenylene fragments have been designed and prepared to understand the interactions in fragment orbitals, the influence of the substituents (F, OMe) on the HOMO-LUMO gap, and th