2-(Tri-n-butylstannyl)thiophene, 97%
2-(Tri-n-butylstannyl)thiophene, 97%
2-(Tri-n-butylstannyl)thiophene, 97%
Thermo Scientific Chemicals

2-(Tri-n-butylstannyl)thiophene, 97%

CAS: 54663-78-4 | C16H30SSn | 373.19 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
5 mL
25 mL
100 mL
This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number H55904.AE
also known as H55904-AE
Price (TWD)
-
Quantity:
100 mL
Request bulk or custom format
Chemical Identifiers
CAS54663-78-4
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Assay (GC)≥96.0%
Identification (FTIR)Conforms
2-(Tri-n-butylstannyl)thiophene derivative is employed in Stille reaction involving efficient carbon-carbon bond formation.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-(Tri-n-butylstannyl)thiophene derivative is employed in Stille reaction involving efficient carbon-carbon bond formation.

Notes
Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Yue, W.; Larsen-Olsen, T. T.; Hu, X.; Shi, M.; Chen, H.; Hinge, M.; Fojan, P.; Krebs, F. C.; Yu, D. Synthesis and photovoltaic properties from inverted geometry cells and roll-to-roll coated large area cells from dithienopyrrole-based donor-acceptor polymers. J. Mater. Chem. A 2013, 1 (5), 1785-1793.
  2. Leliège, A.; Régent, C. H. L.; Allain, M.; Blanchard, P.; Roncali, J. Structural modulation of internal charge transfer in small molecular donors for organic solar cells. Chem. Commun. 2012, 48 (48), 8907-8909.