Tributylstannyltrimethylsilane
Product Information
Molecular Formula
C15H36SiSn
Molecular Weight
363.23
Description
Tributylstannyltrimethylsilane is a vital reagent utilized in the synthesis of diverse pharmaceutical agents that holds paramount importance in the realm of drug development. Its widespread application lies in the creation of organotin-containing medicinal substances, including antibacterial and antifungal agents. Functioning as a versatile ancestral compound, it seamlessly integrates stannyl moieties into drug structures, thereby amplifying their bioactivity and pharmacological attributes.
Synonyms
(Tributylstannyl)trimethylsilane,(Trimethylsilyl)tributylstannane,(Trimethylsilyl)tributyltin,Tributyl(trimethylsilyl)stannane
SMILES
CCCC[Sn](CCCC)CCCC.C[Si](C)C
InChI
InChI=1S/3C4H9.C3H9Si.Sn/c3*1-3-4-21-4(2)3/h3*1,3-4H2,2H31-3H3
InChI Key
MZUUBYSIDDKUKE-UHFFFAOYSA-N
Boiling Point
102-103 °C/0.5 mmHg (lit.)
Flash Point
235.4 °F - closed cup
Purity
96%
Density
1.04 g/mL at 25 °C (lit.)
Refractive Index
n20/D 1.488 (lit.)
Safety Information
Hazards
H301 - H312 - H315 - H319 - H372 - H410
Precautionary Statement
P273 - P280 - P301 + P310 + P330 - P302 + P352 + P312 - P305 + P351 + P338 - P314
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
9
Exact Mass
364.160830 g/mol
Monoisotopic Mass
364.160830 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
17
Formal Charge
0
Complexity
104
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
2
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| WO-2021124097-A1 | Multi-functional hybrid material based on sepiolite for environmental recovery and bio-remediation | 2019-12-19 |
| WO-2021124103-A1 | Multi-functional hybrid material based on natural clays for environmental recovery and bio-remediation | 2019-12-19 |
| WO-2017177922-A1 | Liquid crystal polyester composition | 2016-04-13 |
| WO-2014022377-A1 | Membranes and coatings made from mixtures including ionic liquids having silicon-bonded hydrolyzable groups | 2012-07-30 |
| JP-2013060384-A | METHOD FOR PRODUCING α-AMINO ACID SALT | 2011-09-13 |
| JP-5794569-B2 | Method for producing α-amino acid salt | 2011-09-13 |
| JP-2013049638-A | Method for producing α-hydroxy acid salt | 2011-08-30 |
| JP-5747740-B2 | Method for producing α-hydroxy acid salt | 2011-08-30 |
| EP-2691403-A1 | New boranophosphate analogues of cyclic nucleotides | 2011-03-29 |
| EP-2691403-B1 | New boranophosphate analogues of cyclic nucleotides | 2011-03-29 |
