Cyanomethanethioamide

Base Information

Chemical Name:Cyanomethanethioamide
CAS No.:471-24-9
Molecular Formula:C₂H₂N₂S
Molecular Weight:86.1173
Hs Code.:
DSSTox Substance ID:DTXSID60463612
Nikkaji Number:J1.540.454J

Synonyms:Cyanomethanethioamide;471-24-9;carbamothioyl cyanide;CARBONOCYANIDOTHIOIC AMIDE;Flaveanwasserstoff;DTXSID60463612;AKOS006337434;EN300-84392

Suppliers and Price of Cyanomethanethioamide

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 3 raw suppliers

Chemical Property of Cyanomethanethioamide

Chemical Property:

XLogP3:-0.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:85.99386925
Heavy Atom Count:5
Complexity:87.1

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(#N)C(=S)N

Technology Process of Cyanomethanethioamide

There total 1 articles about Cyanomethanethioamide 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:

: 460-19-5,25215-76-3
ethanedinitrile

: 7783-06-4
hydrogen sulfide

: 471-24-9
cyanothioformamide

: 79-40-3
dithiooxamide

Guidance literature:

Reference yield: 80.0%

: 471-24-9
cyanothioformamide

: 103-71-9
phenyl isocyanate

: bis[2-oxo-1-phenyl-3-(phenylcarbamoyl)-5-(phenylcarbamoylimino)-imidazolidin-4-yl] disulfide

Guidance literature:: With hydrogen sulfide; triethylamine; In diethyl ether; at 25 ℃; for 3h;
DOI:10.1002/1099-0690(200105)2001:9<1695::AID-EJOC1695>3.0.CO;2-0

Reference yield: 55.0%

: 471-24-9
cyanothioformamide

: 104-12-1
p-chlorphenylisocyanate

: bis{1-(4-chlorophenyl)-3-[(4-chlorophenyl)carbamoyl]-5-[(4-chlorophenyl)carbamoylimino]-2-oxoimidazolidin-4-yl} disulfide

Guidance literature:: With hydrogen sulfide; triethylamine; In diethyl ether; at 25 ℃; for 3h;
DOI:10.1002/1099-0690(200105)2001:9<1695::AID-EJOC1695>3.0.CO;2-0