Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione

Base Information

Chemical Name:Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione
CAS No.:73907-94-5
Molecular Formula:C₉H₅N₃O₂
Molecular Weight:187.158
Hs Code.:2933990090
NSC Number:350008
DSSTox Substance ID:DTXSID00419557
Wikidata:Q107944925,Q82230603
Mol file:73907-94-5.mol

Synonyms:Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione;73907-94-5;1,6-dihydropyrrolo[2,3-g]indazole-7,8-dione;NSC350008;SCHEMBL4080527;DTXSID00419557;MFCD03856014;STK774052;AKOS005617510;NSC-350008;CS-0319476;2,6-Dihydropyrrolo[2,3-g]indazole-7,8-dione;A866001;1H,6H,7H,8H-pyrrolo[2,3-g]indazole-7,8-dione;Pyrrolo[2,3-g]indazole-7,8-dione, 1,6-dihydro-

Suppliers and Price of Pyrrolo[2,3-g]indazole-7,8(1H,6H)-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

Crysdot
Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione 95+%
1g
$ 377.00

American Custom Chemicals Corporation
PYRROLO[2,3-G]INDAZOLE-7,8(1H,6H)-DIONE 95.00%
5MG
$ 499.40

Alichem
Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione
1g
$ 400.00

Total 12 raw suppliers

Chemical Property of Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione

Chemical Property:

Vapor Pressure:0.000306mmHg at 25°C
Boiling Point:321°C at 760 mmHg
Flash Point:148°C
PSA：78.61000
Density:1.86g/cm³
LogP:0.20240
Storage Temp.:2-8°C
XLogP3:0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:187.038176411
Heavy Atom Count:14
Complexity:304

Purity/Quality:

97% ^*data from raw suppliers

Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C3=C1C=NN3)C(=O)C(=O)N2

Technology Process of Pyrrolo[2,3-g]indazole-7,8(1H,6H)-dione

There total 5 articles about Pyrrolo[2,3-g]indazole-7,8(1H,6H)-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: 85.0%