Ethynethiol

Base Information

Chemical Name:Ethynethiol
CAS No.:53750-02-0
Molecular Formula:C2H2S
Molecular Weight:58.1039
Hs Code.:
DSSTox Substance ID:DTXSID80405756
Nikkaji Number:J661.248B
Wikidata:Q82210456
Mol file:53750-02-0.mol

Synonyms:Ethynethiol;53750-02-0;DTXSID80405756

Suppliers and Price of Ethynethiol

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
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price

Total 0 raw suppliers

Chemical Property of Ethynethiol

Chemical Property:

Boiling Point:23.5±23.0 °C(Predicted)
PSA：38.80000
Density:0.978±0.06 g/cm3(Predicted)
LogP:0.50690
XLogP3:0.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:57.98772124
Heavy Atom Count:3
Complexity:29.3

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C#CS

Technology Process of Ethynethiol

There total 5 articles about Ethynethiol 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:

: 288-16-4
isothiazol

: 157-20-0
ethylene sulphide

: 74-90-8
hydrogen cyanide

: 18282-77-4
thioketene

: 53750-02-0
ethynethiol

Guidance literature:: In gaseous matrix; at -265.2 ℃; Irradiation; λ = 2500 Angstroem;
DOI:10.1021/ja00393a002

Reference yield:

: 288-48-2
1,2,3-thiadiazole

: 75-15-0,12122-00-8
carbon disulfide

: 18282-77-4
thioketene

: 53750-02-0
ethynethiol

Guidance literature:: In gaseous matrix; at -265.2 ℃; Product distribution; Mechanism; Irradiation; two former products the same in Ar or N₂ matrix; pyrex-filtered photodecomposition in CO matrix and in acetylene-d2 are evidences against free hydrogen and sulphur atoms intermediate formation;
DOI:10.1021/ja00393a002