Trichlorophenylstannane
Product Information
Molecular Formula
C6H5Cl3Sn
Molecular Weight
302.17
Description
Phenyltin trichloride can be used:• In the preparation of organotin(IV) complexes as potent antimicrobial agents.• As a reactant in the Stille coupling reaction catalyzed by peptide-templated Pd nanoparticles.• As a tin (Sn) source in the synthesis of tin-doped TiO2 photoanodes applicable in dye-sensitized solar cells.
Synonyms
PHENYLTRICHLOROSTANNANE; PHENYLTRICHLOROTIN; PHENYLTIN TRICHLORIDE; MONOPHENYLTIN TRICHLORIDE; TRICHLOROPHENYLSTANNANE; Stannane, trichlorophenyl; trichlorophenyl-stannan; trichlorophenyltin
IUPAC Name
trichloro(phenyl)stannane
SMILES
C1=CC=C(C=C1)[Sn](Cl)(Cl)Cl
InChI
InChI=1S/C6H5.3ClH.Sn/c1-2-4-6-5-3-1/h1-5H3*1H/q+3/p-3
InChI Key
UBOGEXSQACVGEC-UHFFFAOYSA-K
Boiling Point
142-143°C
Flash Point
235.4 °F - closed cup
Purity
PRACTICAL
Density
1.839
Appearance
Colorless liquid
Storage
Dark Room
Refractive Index
n20/D 1.585 (lit.)
Safety Information
Hazards
H314 - H400
Precautionary Statement
P273 - P280 - P301 + P330 + P331 - P303 + P361 + P353 - P305 + P351 + P338 + P310
Computed Properties
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
0
Exact Mass
301.847886 g/mol
Monoisotopic Mass
301.847886 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
10
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
1
Compound Is Canonicalized
Yes
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-113860358-A | Method for preparing multi-metal sulfide nanosheets from tanning sulfur-containing wastewater | 2021-10-27 |
| CN-113637296-A | Preparation method of polylactic acid composite material and preparation method of degradable optical film | 2021-07-01 |
| CN-113363427-A | Preparation method of lithium alloy cathode for sulfide all-solid-state battery and battery thereof | 2021-06-07 |
| CN-114057913-A | Solid catalyst component for olefin polymerization | 2020-08-07 |
| DE-102021120168-A1 | SOLID CATALYST COMPONENT FOR OLEFIN POLYMERIZATION | 2020-08-07 |
| JP-2022031142-A | Solid catalyst component for olefin polymerization | 2020-08-07 |
| US-2022041763-A1 | Solid catalyst component for olefin polymerization | 2020-08-07 |
| CN-111926313-A | Composite material of metal zinc foil and zinc-philic crystal nucleus and preparation method and application thereof | 2020-08-05 |
| CN-111926313-B | Composite material of metal zinc foil and zinc-philic crystal nucleus and preparation method and application thereof | 2020-08-05 |
| CN-113999276-A | Purification method and preparation method of deacetyl hairy flower glycoside intermediate | 2020-07-28 |
Literatures
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 17643347 | 2008-03-01 | A UV-vis spectroscopic study of 1:2 adduct formation of some free-base meso-tetraaryl- and meso-tetraalkylporphyrins with PhSnCl3 and (CH3)2SnCl2 | Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy |
