tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide

Base Information

Chemical Name:tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide
CAS No.:140217-84-1
Molecular Formula:C10H17NO5S
Molecular Weight:263
Hs Code.:2934999090
DSSTox Substance ID:DTXSID601119440
Mol file:140217-84-1.mol

Synonyms:tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide;140217-84-1;tert-butyl 1,1,6-trioxo-1,4-thiazepane-4-carboxylate;ZIOHMVIJBJPTBH-UHFFFAOYSA-N;SCHEMBL7410120;DTXSID601119440;AT40039;DB-353085;A898462;tert-butyl 1,1,6-trioxo-1lambda,4-thiazepane-4-carboxylate;4-N-(t-Butyloxycarbonyl)-1,1-dioxo -2,3,4,5,6,7-hexahydro-1,4-thiazepin-6-one;1,4-Thiazepine-4(5H)-carboxylic acid, tetrahydro-6-oxo-, 1,1-dimethylethyl ester, 1,1-dioxide

Suppliers and Price of tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide

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 tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide

Chemical Property:

PSA：89.13000
LogP:1.23970
XLogP3:0.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:263.08274382
Heavy Atom Count:17
Complexity:415

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC(=O)N1CCS(=O)(=O)CC(=O)C1

Technology Process of tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide

There total 1 articles about tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide 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:

: 140217-84-1
4-N-(t-butyloxycarbonyl)-1,1-dioxo-2,3,4,5,6,7-hexahydro-1,4-thiazepin-6-one

Guidance literature:

Reference yield: 50.0%

: 1,1-dioxothiazepinone

: 140217-84-1
4-N-(t-butyloxycarbonyl)-1,1-dioxo-2,3,4,5,6,7-hexahydro-1,4-thiazepin-6-one

: 54527-73-0
2-(N-benzyl-N-methylamino)-ethyl 3-aminocrotonate

: 6334-18-5
2,3-dichlorobenzylaldehyde

: 2-(N-benzyl-N-methylamino)ethyl 4-t-butyloxycarbonyl-9-(2,3-dichlorophenyl)-1,1-dioxo-5a-hydroxy-2,3,4,5,5a,6,9,9a-octahydro-7-methylpyrido[2,3-f][1,4]thiazepine-8-carboxylate

Guidance literature:: In ethanol;

Reference yield:

: 140217-84-1
4-N-(t-butyloxycarbonyl)-1,1-dioxo-2,3,4,5,6,7-hexahydro-1,4-thiazepin-6-one

: ethyl 9-(2,3-dichlorophenyl)-1,1-dioxo-2,3,4,5,6,9-hexahydro-7-methyl-pyrido[2,3-f][1,4]thiazepine-8-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: ethanol; toluene

2: sodium hydroxide / ethyl acetate

With sodium hydroxide; In ethanol; ethyl acetate; toluene;