CID 5381446

Base Information

Chemical Name:CID 5381446
CAS No.:18006-04-7
Molecular Formula:C₁₂H₁₁ClSn
Molecular Weight:309.382
Hs Code.:
DSSTox Substance ID:DTXSID20297778
Mol file:18006-04-7.mol

Synonyms:18006-04-7;AC1L6SOW;SCHEMBL7053057;SCHEMBL7937450;DTXSID20297778

Suppliers and Price of CID 5381446

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 0 raw suppliers

Chemical Property of CID 5381446

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:2
Exact Mass:308.949306
Heavy Atom Count:14
Complexity:142

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)[Sn](C2=CC=CC=C2)Cl

Technology Process of CID 5381446

There total 2 articles about CID 5381446 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 688-73-3
tri-n-butyl-tin hydride

: 1135-99-5
diphenyltin(IV) dichloride

: 18006-04-7
chlorodiphenyltin hydride

Guidance literature:: In not given; reaction in a mol-ratio of 1:1;;
DOI:10.1016/0022-328X(68)80038-5

Reference yield:

: 16853-85-3
lithium aluminium tetrahydride

: 1135-99-5
diphenyltin(IV) dichloride

: 18006-04-7
chlorodiphenyltin hydride

Guidance literature:: In not given; according to J. Appl. Chem. 1957, 7, 366;
DOI:10.1021/om200987t

Reference yield: 95.0%

: 18006-04-7
chlorodiphenyltin hydride

: 922-67-8
propynoic acid methyl ester

: 203380-25-0
(C₆H₅)2ClSnCHCHCOOCH₃

Guidance literature:: With 2,2'-azobis(isobutyronitrile); In benzene; org. compd. addn. to Sn-compd. soln. with traces of azoisobutyronitrile (Ar), mixt. heating cautiously to 55°C for 2 h (stirring), further stirring at room temp. for 15 h, concn. (reduced pressure);