1H-Benz[g]indole-2,3-dione

Base Information

Chemical Name:1H-Benz[g]indole-2,3-dione
CAS No.:5353-96-8
Molecular Formula:C12H7 N O2
Molecular Weight:197.1895
Hs Code.:2933990090
DSSTox Substance ID:DTXSID30201745
Nikkaji Number:J38.211F
Wikidata:Q83074956
Mol file:5353-96-8.mol

Synonyms:1H-Benz[g]indole-2,3-dione;5353-96-8;Benzo[g]isatin;1H-benzo[g]indole-2,3-dione;Benz(g)isatin;1H-Benz(g)indole-2,3-dione;benz[g]isatin;BRN 0150030;4-21-00-05553 (Beilstein Handbook Reference);benzindolequinone;SCHEMBL458053;DTXSID30201745;AC6314;MFCD01658932;AKOS000147988;LS-33455;SY058407;A917933

Suppliers and Price of 1H-Benz[g]indole-2,3-dione

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

American Custom Chemicals Corporation
1H-BENZO[G]INDOLE-2,3-DIONE 95.00%
5MG
$ 502.18

AK Scientific
1H-Benz[g]indole-2,3-dione
1g
$ 458.00

Total 4 raw suppliers

Chemical Property of 1H-Benz[g]indole-2,3-dione

Chemical Property:

Melting Point:260-262 °C (decomp)
Boiling Point:°Cat760mmHg
PKA:9.33±0.20(Predicted)
Flash Point:°C
PSA：46.17000
Density:1.391 g/cm³
LogP:2.11260
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:197.047678466
Heavy Atom Count:15
Complexity:313

Purity/Quality:

97% ^*data from raw suppliers

1H-BENZO[G]INDOLE-2,3-DIONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C(=C1)C=CC3=C2NC(=O)C3=O

Technology Process of 1H-Benz[g]indole-2,3-dione

There total 1 articles about 1H-Benz[g]indole-2,3-dione 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:

: 5353-96-8
6,7-benzoisatin

: 5810-96-8
benzisatin

Guidance literature:

Reference yield: 66.0%

: 5353-96-8
6,7-benzoisatin

: 40207-03-2
p-Anisidinothioformyl-hydrazin

: 1155338-46-7
1-(1H'-benz[g]indole-2',3'-dione)-4(4'-methoxyphenyl)-3-semicarbazone

Guidance literature:: With acetic acid; In ethanol; Reflux;
DOI:10.1021/jm800861c

Reference yield: 63.0%

: 5353-96-8
6,7-benzoisatin

: 501-65-5
diphenyl acetylene

: 1424352-16-8
8,9,10-triphenyl-7H-benzo[g]pyrrolo[1,2-a]indol-7-one

Guidance literature:: With silver(I) acetate; palladium diacetate; In 1,4-dioxane; acetonitrile; at 100 ℃; for 30h; Inert atmosphere;
DOI:10.1002/anie.201208076