dimethyl(diprop-2-en-1-yl)stannane

Base Information

Chemical Name:dimethyl(diprop-2-en-1-yl)stannane
CAS No.:19434-15-2
Molecular Formula:C8H16 Sn
Molecular Weight:230.925
Hs Code.:
Mol file:19434-15-2.mol

Synonyms:Stannane,diallyldimethyl- (8CI); Stannane, dimethyldi-2-propenyl- (9CI);Diallyldimethylstannane; NSC 348065

Suppliers and Price of dimethyl(diprop-2-en-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 4 raw suppliers

Chemical Property of dimethyl(diprop-2-en-1-yl)stannane

Chemical Property:

Vapor Pressure:1.68mmHg at 25°C
Boiling Point:173.6°C at 760 mmHg
Flash Point:54.1°C

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of dimethyl(diprop-2-en-1-yl)stannane

There total 4 articles about dimethyl(diprop-2-en-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: 78.0%

: 753-73-1
dimethyltin dichloride

: 1730-25-2
allylmagnesium bromide

: 19434-15-2
dimethyldiallyltin

Guidance literature:: In diethyl ether; at 0°C;;
DOI:10.1039/DT9730001706

Reference yield:

: 762-73-2
trimethyl(allyl)stannane

: 109-63-7
trifluoroborane diethyl ether

: 594-27-4
tetramethylstannane

: 19713-79-2
triallylmethylstannane

: 19434-15-2
dimethyldiallyltin

Guidance literature:: In chloroform-d1; dichloromethane-d2; CDCl3/CD2Cl2 = 1:1 at 0.5 M at -80°C; signals ((13)C-NMR) for (CH3)4Sn were visible at -20°C, upon recooling to -80°C redistribution of the allyl groups; (13)C-NMR, the identical spectrum could be obtained by reaction of Me4Sn and (allyl)4Sn with BF3*OEt2 (-80/+20/-80°C);
DOI:10.1021/ja00211a058