(tert-Butoxyethynesulfonyl)benzene

Base Information

Chemical Name:(tert-Butoxyethynesulfonyl)benzene
CAS No.:79894-53-4
Molecular Formula:C12H14O3S
Molecular Weight:238.307
Hs Code.:
DSSTox Substance ID:DTXSID10507772

Synonyms:79894-53-4;(tert-Butoxyethynesulfonyl)benzene;DTXSID10507772;[(tert-butoxyethynyl)sulfonyl]benzene;2-tert-butoxy-ethynylsulfonyl-benzene

Suppliers and Price of (tert-Butoxyethynesulfonyl)benzene

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 1 raw suppliers

Chemical Property of (tert-Butoxyethynesulfonyl)benzene

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:238.06636548
Heavy Atom Count:16
Complexity:378

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)(C)OC#CS(=O)(=O)C1=CC=CC=C1

Technology Process of (tert-Butoxyethynesulfonyl)benzene

There total 4 articles about (tert-Butoxyethynesulfonyl)benzene 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: 76.0%

: 3559-73-7
phenyl 2,2-dichlorovinyl sulfone

: 865-47-4
potassium tert-butylate

: 79894-53-4
tert-butoxyethynyl phenyl sulfone

Guidance literature:: In tetrahydrofuran; at -70 ℃; for 1h;

Reference yield:

: 6618-71-9
2,2,2-trichloroethyl phenyl sulfone

: 79894-53-4
tert-butoxyethynyl phenyl sulfone

Guidance literature:: Multi-step reaction with 2 steps

1: 63.2 percent / triethylamine / benzene / 4 h / Heating

2: 76 percent / tetrahydrofuran / 1 h / -70 °C

With triethylamine; In tetrahydrofuran; benzene;

Reference yield:

: 56354-48-4
2,2,2-trichloroethyl phenyl sulfide

: 79894-53-4
tert-butoxyethynyl phenyl sulfone

Guidance literature:: Multi-step reaction with 3 steps

1: 81.4 percent / potassium permanganate / acetic acid / Ambient temperature

2: 63.2 percent / triethylamine / benzene / 4 h / Heating

3: 76 percent / tetrahydrofuran / 1 h / -70 °C

With potassium permanganate; triethylamine; In tetrahydrofuran; acetic acid; benzene;