S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

Base Information

Chemical Name:S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride
CAS No.:438047-08-6
Molecular Formula:C₁₅H₂₁N₃O₃S*ClH
Molecular Weight:359.877
Hs Code.:

Synonyms:S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

Suppliers and Price of S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

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 S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

There total 2 articles about S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride 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: 58.6%

: 438049-39-9
S-4-hydroxybenzyl 4-tert-butoxycarbonylpiperazine-1-thiocarboxylate

: 109-90-0
ethyl isocyanate

: 438047-08-6
S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

Guidance literature:

Reference yield:

: 438049-38-8
[(4-tert-butyl-dimethylsilyloxy)benzylsulfanylcarbonyl]-piperazine-4-carboxylic acid tert-butyl ester

: 438047-08-6
S-4-[(Ethylamino)carbonyl]oxybenzyl piperazine-1-thiocarboxylate hydrochloride

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutyl ammonium fluoride / tetrahydrofuran

With tetrabutyl ammonium fluoride; In tetrahydrofuran;