Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane

Base Information

Chemical Name:Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane
CAS No.:1251-10-1
Molecular Formula:C₂₈H₂₀Sn
Molecular Weight:475.177
Hs Code.:
DSSTox Substance ID:DTXSID10523533
Wikidata:Q82389682

Synonyms:1251-10-1;Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane;DTXSID10523533

Suppliers and Price of Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane

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
Packaging
price

Total 2 raw suppliers

Chemical Property of Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane

Chemical Property:

Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:0
Rotatable Bond Count:6
Exact Mass:476.058703
Heavy Atom Count:29
Complexity:579

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C#CC#C[Sn](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4

Technology Process of Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane

There total 5 articles about Triphenyl(4-phenylbuta-1,3-diyn-1-yl)stannane 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: 55.0%

: 5701-81-5
buta-1,3-diynylbenzene

: 894-09-7
iodotriphenylstannane

: 1251-10-1
Triphenyl-phenylbutadiinylstannan

Guidance literature:: With sodium; In ammonia; 2 h;;

Reference yield:

: 639-58-7
triphenyltin chloride

: 1251-10-1
Triphenyl-phenylbutadiinylstannan

Guidance literature:: Multi-step reaction with 5 steps

1: benzene

2: Br₂

3: tetrahydrofuran

4: I₂

5: Na / ammonia

With Br₂; I₂; Na; In tetrahydrofuran; ammonia; benzene;