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1135-99-5,MFCD00000516
Catalog No.:AA0008P7

1135-99-5 | Stannane, dichlorodiphenyl-

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1g
95%
in stock  
$24.00   $17.00
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5g
95%
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$51.00   $36.00
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50g
96%
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$471.00   $330.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0008P7
Chemical Name:
Stannane, dichlorodiphenyl-
CAS Number:
1135-99-5
Molecular Formula:
C12H10Cl2Sn
Molecular Weight:
343.8148
MDL Number:
MFCD00000516
SMILES:
Cl[Sn](c1ccccc1)(c1ccccc1)Cl
NSC Number:
405640
Properties
Properties
 
BP:
330.7°C at 760 mmHg  
Form:
Solid  
MP:
41-43℃  
Storage:
2-8℃;Keep in dry area;  

Computed Properties
 
Complexity:
174  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
15  
Rotatable Bond Count:
2  

Downstream Synthesis Route
379-50-0    1135-99-5    7439-95-4   
MgClF 
 
Ph3SiSnPh2SiPh3 

[1]JournalofOrganometallicChemistry,2003,vol.686,p.332-340

938-33-0    1135-99-5   
1,3-dichloro-1,1,3,3-tetraphenyldistannaoxane 
 
bis(8-methoxyquinolinium)tetrachlorodiphenylstannate(IV) 

[1]JournalofOrganometallicChemistry,1998,vol.561,p.143-152

938-33-0    1135-99-5   
1,3-dichloro-1,1,3,3-tetraphenyldistannaoxane 
 
bis(8-methoxyquinolinium)tetrachlorodiphenylstannate(IV) 
 
(8-methoxyquinolium)(8-methoxyquinoline)Ph2SnCl3 

[1]JournalofOrganometallicChemistry,1998,vol.561,p.143-152

7298-84-2    1135-99-5   
(phenyl)2Sn(leucylalanine(2-)) 

[1]Nath,Mala;Pokharia,Sandeep;Eng,George;Song,Xueqing;Kumar,Ashok[SynthesisandReactivityinInorganicandMetal-OrganicChemistry,2004,vol.34,#10,p.1689-1708]

1135-99-5    25700-11-2   
(diphenyl)tinCl2{1-(2-pyridyl)pyrazole} 

[1]IndianJournalofChemistry,SectionA:Inorganic,Physical,TheoreticalandAnalytical,1989,vol.28,p.51-54

Literature

Title: Identification of inhibitors of drug-resistant Candida albicans strains from a library of bicyclic peptidomimetic compounds.

Journal: Journal of medicinal chemistry 20100325

Title: Synthesis, characterization and biocidal activity of new organotin complexes of 2-(3-oxocyclohex-1-enyl)benzoic acid.

Journal: European journal of medicinal chemistry 20100301

Title: Structure-dependent activation of peroxisome proliferator-activated receptor (PPAR) gamma by organotin compounds.

Journal: Chemico-biological interactions 20090715

Title: Antioxidative effect of quercetin and its equimolar mixtures with phenyltin compounds on liposome membranes.

Journal: Journal of agricultural and food chemistry 20061004

Title: Trialkyltin compounds bind retinoid X receptor to alter human placental endocrine functions.

Journal: Molecular endocrinology (Baltimore, Md.) 20051001

Title: Synthesis and structure-activity correlation studies of metal complexes of alpha-N-heterocyclic carboxaldehyde thiosemicarbazones in Shewanella oneidensis.

Journal: International journal of environmental research and public health 20050501

Title: 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: Journal of chromatography. A 20050422

Title: Suppression of uterine decidualization correlated with reduction in serum progesterone levels as a cause of preimplantation embryonic loss induced by diphenyltin in rats.

Journal: Reproductive toxicology (Elmsford, N.Y.) 20020101

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