trans-1,2-Bis(tri-n-butylstannyl)ethylene, 96%
trans-1,2-Bis(tri-n-butylstannyl)ethylene, 96%
trans-1,2-Bis(tri-n-butylstannyl)ethylene, 96%
Thermo Scientific Chemicals

trans-1,2-Bis(tri-n-butylstannyl)ethylene, 96%

CAS: 14275-61-7 | C26H56Sn2 | 606.154 g/mol
製品番号(カタログ番号) L20130.06
または、製品番号L20130-06
価格(JPY)
-
数量:
5 g
一括またはカスタム形式をリクエストする
化学物質識別子
CAS14275-61-7
IUPAC Nametributyl[2-(tributylstannyl)ethenyl]stannane
Molecular FormulaC26H56Sn2
InChI KeyVNKOWRBFAJTPLS-UHFFFAOYSA-N
SMILESCCCC[Sn](CCCC)(CCCC)C=C[Sn](CCCC)(CCCC)CCCC
さらに表示
FormLiquid
Proton NMRConforms to structure
Appearance (Color)Clear colorless to pale yellow
Identification (FTIR)Conforms
Assay by NMR≥95.0%
trans-1,2-Bis(tri-n-butylstannyl)ethylene is used as an intermediate in organic synthesis. It is also employed in the synthesis of gamma, delta-alkynones.

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
trans-1,2-Bis(tri-n-butylstannyl)ethylene is used as an intermediate in organic synthesis. It is also employed in the synthesis of gamma, delta-alkynones.

Solubility
Miscible with terahydrofuran and dimethyl formamide. Slightly miscible with water.

Notes
Store in a cool place. Incompatible with strong oxidizing agents.
RUO – Research Use Only

General References:

  1. Liu, Y.; Liu, Z.; Luo, H.; Xie, X.; Ai, L.; Ge, Z.; Yu, G.; Liu, Y. Benzothieno [2, 3-b] thiophene semiconductors: synthesis, characterization and applications in organic field-effect transistors. J. Mater. Chem. 2014, 2 (41), 8804-8810.
  2. Kim, J.; Han, A. R.; Hong, J.; Kim, G.; Lee, J.; Shin, T. J.; Oh, J. H.; Yang, C. Ambipolar Semiconducting Polymers with π-Spacer Linked Bis-Benzothiadiazole Blocks as Strong Accepting Units. Chem. Mater. 2014, 26 (17), 4933-4942.