N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

Base Information

Chemical Name:N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine
CAS No.:1067073-38-4
Molecular Formula:C₁₂H₂₀B₁₀F₃NO₄S
Molecular Weight:439.466
Hs Code.:

Synonyms:

Suppliers and Price of N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

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 0 raw suppliers

Chemical Property of N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

There total 2 articles about N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine 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:

: 107651-35-4
methyl 3,3,3-trifluoro-2-benzenesulfonyliminopropionate

: 1067073-38-4
N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

Guidance literature:: Multi-step reaction with 2 steps

1: water; diethyl ether

2: water; tetrahydrofuran

In tetrahydrofuran; diethyl ether; water;
DOI:10.1007/s11172-007-0118-9

Reference yield:

: 737767-06-5
methyl N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalaninate

: 1310-65-2
lithium hydroxide

: 1067073-38-4
N-(phenylsulfonyl)-α-(trifluoromethyl)-o-carboranylalanine

Guidance literature:: In tetrahydrofuran; water; B compd. added to soln. of LiOH in THF-H2O; stirred at 20°C for 4d; extd. with benzene; 1 M HCl added to aq. layer; ppt. extd. with Et2O; dried (anhyd. Na2SO4); solvent removed;
DOI:10.1007/s11172-007-0118-9