Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-

Base Information

Chemical Name:Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-
CAS No.:537710-19-3
Molecular Formula:C21H35NO3Sn
Molecular Weight:468.224
Hs Code.:
DSSTox Substance ID:DTXSID80467930

Synonyms:537710-19-3;Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-;DTXSID80467930

Suppliers and Price of Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-

Supply Marketing:

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

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Chemical Property of Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:13
Exact Mass:469.163897
Heavy Atom Count:26
Complexity:392

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC[Sn](CCCC)(CCCC)C(=C)COC1=CC=C(C=C1)[N+](=O)[O-]

Technology Process of Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]-

There total 1 articles about Stannane, tributyl[1-[(4-nitrophenoxy)methyl]ethenyl]- 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: 62.0%

: 17061-85-7
1-nitro-4-(prop-2-ynyloxy)benzene

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

: 897027-90-6
O₂NC₆H₄OCH₂CHCHSn(C₄H₉)3

: 537710-19-3
O₂NC₆H₄OCH₂C(CH₂)Sn(C₄H₉)3

: 537710-13-7
O₂NC₆H₄OCH₂C[Sn(C₄H₉)3]CHSn(C₄H₉)3

Guidance literature:: With hydroquinone; (CO)5W[CNC₆H₄NO₂]; In toluene; byproducts: (Bu3Sn)2; alkyne and catalyst with hydroquinone dissolved in abs. toluene, heated for 15 min at 60°C, Bu3SnH added, heated for 12 h at 60°C; solv. removed, chromy over silica gel with pure hexane, then hexane/ethyl acetate/1% triethylamine, 98-90% hexane;
DOI:10.1002/anie.200390102