2-(Tributylstannyl)thiophene - CAS 54663-78-4
Catalog: |
BB028755 |
Product Name: |
2-(Tributylstannyl)thiophene |
CAS: |
54663-78-4 |
Synonyms: |
tributyl(thiophen-2-yl)stannane; tributyl(thiophen-2-yl)stannane |
IUPAC Name: | tributyl(thiophen-2-yl)stannane |
Description: | 2-(Tributylstannyl)thiophene has been used to synthesize diphenylquinoxaline monomer for the electrochromism polymers. It can also be used as a reactant in Stille coupling reaction. |
Molecular Weight: | 373.18 |
Molecular Formula: | C16H30SSn |
Canonical SMILES: | CCCC[Sn](CCCC)(CCCC)C1=CC=CS1 |
InChI: | InChI=1S/C4H3S.3C4H9.Sn/c1-2-4-5-3-1;3*1-3-4-2;/h1-3H;3*1,3-4H2,2H3; |
InChI Key: | UKTDFYOZPFNQOQ-UHFFFAOYSA-N |
Boiling Point: | 155 °C / 0.1 mmHg (lit.) |
Flash Point: | 221.0 °F - closed cup |
Purity: | 97 % |
Density: | 1.175 g/mL at 25 °C (lit.) |
MDL: | MFCD00192513 |
LogP: | 5.80420 |
Refractive Index: | n20/D 1.518 (lit.) |
GHS Hazard Statement: | H301 (100%): Toxic if swallowed [Danger Acute toxicity, oral] |
Precautionary Statement: | P260, P264, P270, P273, P280, P301+P310, P302+P352, P305+P351+P338, P312, P314, P321, P322, P330, P332+P313, P337+P313, P362, P363, P391, P405, and P501 |
Signal Word: | Danger |
Publication Number | Title | Priority Date |
CN-113087876-A | Free radical polymer and application thereof | 20210401 |
CN-112898711-A | Preparation method of high-strength acrylate rubber material | 20210329 |
CN-113061235-A | Copolymer and organic photovoltaic element | 20210322 |
CN-113024779-A | Application of p-type D-A copolymer containing quinoxaline unit in high-efficiency organic and perovskite solar cell | 20210305 |
KR-102308854-B1 | The pharmaceutical composition for prevention and treatment of coronavirus disease-19 containing carbocyclic nucleosides derivatives | 20210226 |
PMID | Publication Date | Title | Journal |
21898622 | 20111010 | In search of oligo(2-thienyl)-substituted pyridine derivatives: a modular approach to di-, tri- and tetra(2-thienyl)pyridines | Chemistry (Weinheim an der Bergstrasse, Germany) |
19821458 | 20091116 | Pd(0)-Mediated rapid coupling between methyl iodide and heteroarylstannanes: an efficient and general method for the incorporation of a positron-emitting (11)C radionuclide into heteroaromatic frameworks | Chemistry (Weinheim an der Bergstrasse, Germany) |
11514175 | 20010820 | Synthesis of 6-(2-thienyl)purine nucleoside derivatives that form unnatural base pairs with pyridin-2-one nucleosides | Bioorganic & medicinal chemistry letters |
Complexity: | 184 |
Compound Is Canonicalized: | Yes |
Covalently-Bonded Unit Count: | 1 |
Defined Atom Stereocenter Count: | 0 |
Defined Bond Stereocenter Count: | 0 |
Exact Mass: | 374.109025 |
Formal Charge: | 0 |
Heavy Atom Count: | 18 |
Hydrogen Bond Acceptor Count: | 1 |
Hydrogen Bond Donor Count: | 0 |
Isotope Atom Count: | 0 |
Monoisotopic Mass: | 374.109025 |
Rotatable Bond Count: | 10 |
Topological Polar Surface Area: | 28.2 Å2 |
Undefined Atom Stereocenter Count: | 0 |
Undefined Bond Stereocenter Count: | 0 |
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