form
powder or crystals
reaction suitability
reaction type: C-C Bond Formation
mp
53-56
storage temp.
2-8°C
Application
Benzene-1,3,5-triyl triformate (TFBen) has been demonstrated to be an efficient and non-reacting CO source for carbonylation reactions in the lab of Xiao-Feng Wu.
Other Notes
Benzene-1,3,5-triyl triformate (TFBen): a convenient, efficient, and non-reacting CO source in carbonylation reactions
A general and practical Lewis acids-catalyzed aryl formates synthesis
DBU-promoted carbonylative synthesis of 1,3-oxathiolan-2-ones from propargylic alcohols with TFBen as the CO source
Base-Promoted Sulfur-Mediated Carbonylative Cyclization of Propargylic Amines
A general and practical Lewis acids-catalyzed aryl formates synthesis
DBU-promoted carbonylative synthesis of 1,3-oxathiolan-2-ones from propargylic alcohols with TFBen as the CO source
Base-Promoted Sulfur-Mediated Carbonylative Cyclization of Propargylic Amines
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
A general and practical Lewis acids-catalyzed aryl formates synthesis.
Jiang LB , et al.
Molecular Catalysis, 433, 8-11 (2017)
Base-Promoted Sulfur-Mediated Carbonylative Cyclization of Propargylic Amines.
Ying J, et al.
European Journal of Organic Chemistry, 2018(5), 688-692 (2018)
Benzene-1,3,5-triyl triformate (TFBen): a convenient, efficient, and non-reacting CO source in carbonylation reactions.
Jiang LB, et al.
Tetrahedron Letters, 57, 3368-3370 (2016)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 901821-1G | 04061835508488 |