sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Base Information

Chemical Name:sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester
CAS No.:914082-85-2
Molecular Formula:C₁₃H₁₇F₃N₂O₅S₂
Molecular Weight:402.416
Hs Code.:

Synonyms:sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Suppliers and Price of sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

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 sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

There total 3 articles about sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester 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:

: 1021374-30-0
[1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-yl]-methanol

: 914082-85-2
sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Guidance literature:: With pyridine; sulphamoyl chloride; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/ol061649x

Reference yield:

: 2991-42-6
4-trifluorophenylsulfonyl chloride

: 914082-85-2
sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: acetone; H₂O / 20 °C

2: ClSO₂NH₂; pyridine / CH₂Cl₂ / 0 - 20 °C

With pyridine; sulphamoyl chloride; In dichloromethane; water; acetone;
DOI:10.1021/ol061649x

Reference yield:

: 3433-37-2
piperidin-2-ylmethanol

: 914082-85-2
sulfamic acid 1-(4-trifluoromethyl-benzenesulfonyl)-piperidin-2-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: acetone; H₂O / 20 °C

2: ClSO₂NH₂; pyridine / CH₂Cl₂ / 0 - 20 °C

With pyridine; sulphamoyl chloride; In dichloromethane; water; acetone;
DOI:10.1021/ol061649x