[(Tert-butoxyethynyl)sulfanyl]benzene

Base Information

Chemical Name:[(Tert-butoxyethynyl)sulfanyl]benzene
CAS No.:79894-50-1
Molecular Formula:C12H14OS
Molecular Weight:206.309
Hs Code.:
DSSTox Substance ID:DTXSID80507769
Wikidata:Q82364181

Synonyms:[(tert-butoxyethynyl)sulfanyl]benzene;79894-50-1;DTXSID80507769;2-tert-butoxy-ethynylsulfanyl-benzene

Suppliers and Price of [(Tert-butoxyethynyl)sulfanyl]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-butoxyethynyl)sulfanyl]benzene

Chemical Property:

XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:206.07653624
Heavy Atom Count:14
Complexity:222

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)(C)OC#CSC1=CC=CC=C1

Technology Process of [(Tert-butoxyethynyl)sulfanyl]benzene

There total 3 articles about [(Tert-butoxyethynyl)sulfanyl]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: 81.6%

: 3559-72-6
1,1-dichloro-2-phenylthioethene

: 865-47-4
potassium tert-butylate

: 79894-50-1
tert-butoxyethynyl phenyl sulfide

Guidance literature:: In tetrahydrofuran; at -40 - -30 ℃; for 0.5h;

Reference yield:

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

: 79894-50-1
tert-butoxyethynyl phenyl sulfide

Guidance literature:: Multi-step reaction with 2 steps

1: 82.3 percent / triethylamine / benzene / 48 h / Heating

2: 81.6 percent / tetrahydrofuran / 0.5 h / -40 - -30 °C

With triethylamine; In tetrahydrofuran; benzene;

Reference yield:

: 931-59-9
benzenesulfenyl chloride

: 79894-50-1
tert-butoxyethynyl phenyl sulfide

Guidance literature:: Multi-step reaction with 3 steps

1: 67.4 percent / iodine / benzene / 5/10 deg C, 20/25 deg C

2: 82.3 percent / triethylamine / benzene / 48 h / Heating

3: 81.6 percent / tetrahydrofuran / 0.5 h / -40 - -30 °C

With iodine; triethylamine; In tetrahydrofuran; benzene;