(3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone

Base Information

Chemical Name:(3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone
CAS No.:4341-57-5
Molecular Formula:C9H7IN4OS
Molecular Weight:346.1476
Hs Code.:
DSSTox Substance ID:DTXSID60195845
Nikkaji Number:J2.025.457B
Wikidata:Q83068900
ChEMBL ID:CHEMBL119370
Mol file:4341-57-5.mol

Synonyms:CHEMBL119370;4341-57-5;Hydrazinecarbothioamide, 2-(1,2-dihydro-5-iodo-2-oxo-3H-indo-3-ylidene)-;(3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone;5-Iodoisatin-3-hydrazinecarbothioamide;DTXSID60195845;CYMDOKFQHWMYFB-UHFFFAOYSA-N;BDBM50133630;2-(1,2-Dihydro-5-iodo-2-oxo-3H-indo-3-ylidene)hydrazinecarbothioamide;AKOS000362099;SR-01000316175;2-(5-Iodo-2-oxoindolin-3-ylidene)thiosemicarbazone;SR-01000316175-1;(3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone #;2-(5-Iodo-2-oxoindolin-3-ylidene)hydrazinecarbothioamide

Suppliers and Price of (3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone

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 (3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone

Chemical Property:

Vapor Pressure:2.3E-06mmHg at 25°C
Boiling Point:392.4°Cat760mmHg
Flash Point:191.1°C
Density:2.23g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:345.93853
Heavy Atom Count:16
Complexity:314

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1I)C(=C(N2)O)N=NC(=S)N

Technology Process of (3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone

There total 2 articles about (3Z)-5-Iodo-1H-indole-2,3-dione 3-thiosemicarbazone 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: 78.0%

: 20780-76-1
5-iodoisatin

: 79-19-6
thiosemicarbazide

: 4341-57-5
C₉H₇IN₄OS

Guidance literature:: at 50 ℃; for 0.5h;

Reference yield:

: 540-37-4
p-aminoiodobenzene

: 4341-57-5
C₉H₇IN₄OS

Guidance literature:: Multi-step reaction with 2 steps

1: 18 percent / hydroxylamine hydrochloride

2: 78 percent / 0.5 h / 50 °C

With hydroxylamine hydrochloride;