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
Canonical 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
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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