Diphenyltin dichloride

Product Information

Molecular Formula:
C12H10Cl2Sn
Molecular Weight:
343.82
Description
Diphenyltin dichloride is an eminent compound within the biomedical realm. As an organometallic reagent, its uninhibited utility manifests during pharmaceutical drug synthesis. Employed diligently in combatting formidable maladies like cancer and fungal infections, its multifaceted nature garners profound admiration.
Synonyms
Dichlorodiphenyltin
IUPAC Name
dichloro(diphenyl)stannane
Canonical SMILES
C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)(Cl)Cl
InChI
InChI=1S/2C6H5.2ClH.Sn/c2*1-2-4-6-5-3-1;;;/h2*1-5H;2*1H;/q;;;;+2/p-2
InChI Key
ISXUHJXWYNONDI-UHFFFAOYSA-L
Boiling Point
333-337°C
Melting Point
41-43°C
Flash Point
235.4 °F - closed cup
Purity
95%
Appearance
white to off-white crystalline powder

Safety Information

Hazards
H302 + H312 + H332 - H315 - H319 - H335 - H400
Precautionary Statement
P273 - P280 - P301 + P312 + P330 - P302 + P352 + P312 - P304 + P340 + P312 - P305 + P351 + P338

Computed Properties

Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
2
Exact Mass
343.918158 g/mol
Monoisotopic Mass
343.918158 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
15
Formal Charge
0
Complexity
174
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-113816988-A Synthetic method of triphenyl tin acetate 2021-10-25
CN-113637296-A Preparation method of polylactic acid composite material and preparation method of degradable optical film 2021-07-01
CN-113025379-A Coking inhibitor for advanced catalytic cracking olefin preparation device and preparation method thereof 2021-02-04
CN-114057913-A 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
CN-111766319-A Method for simultaneously determining contents of tin and lead in different forms in tobacco 2020-07-14

Literatures

PMID Publication Date Title Journal
31706034 2020-02-01 Interaction of organotin compounds with three major glutathione S-transferases in zebrafish Toxicology in vitro : an international journal published in association with BIBRA
20184325 2010-03-25 Identification of inhibitors of drug-resistant Candida albicans strains from a library of bicyclic peptidomimetic compounds Journal of medicinal chemistry
19959261 2010-03-01 Synthesis, characterization and biocidal activity of new organotin complexes of 2-(3-oxocyclohex-1-enyl)benzoic acid European journal of medicinal chemistry
19497422 2009-07-15 Structure-dependent activation of peroxisome proliferator-activated receptor (PPAR) gamma by organotin compounds Chemico-biological interactions
17002447 2006-10-04 Antioxidative effect of quercetin and its equimolar mixtures with phenyltin compounds on liposome membranes Journal of agricultural and food chemistry
15941851 2005-10-01 Trialkyltin compounds bind retinoid X receptor to alter human placental endocrine functions Molecular endocrinology (Baltimore, Md.)
15881455 2005-04-22 New approach of solid-phase microextraction improving the extraction yield of butyl and phenyltin compounds by combining the effects of pressure and type of agitation Journal of chromatography. A
16705815 2005-04-01 Synthesis and structure-activity correlation studies of metal complexes of alpha-N-heterocyclic carboxaldehyde thiosemicarbazones in Shewanella oneidensis International journal of environmental research and public health
12128105 2002-05-01 Suppression of uterine decidualization correlated with reduction in serum progesterone levels as a cause of preimplantation embryonic loss induced by diphenyltin in rats Reproductive toxicology (Elmsford, N.Y.)
5842 1976-05-01 Bile canalicular alkaline phosphatase and disease Acta pathologica et microbiologica Scandinavica. Section A, Pathology
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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