5-Nitroindazole

Base Information

Chemical Name:5-Nitroindazole
CAS No.:5401-94-5
Molecular Formula:C7H5N3O2
Molecular Weight:163.136
Hs Code.:29339990
European Community (EC) Number:226-451-5
NSC Number:5032
UNII:235Y7P37ZD
DSSTox Substance ID:DTXSID5049316
Nikkaji Number:J2.232B
Wikidata:Q27253724
Metabolomics Workbench ID:148978
ChEMBL ID:CHEMBL165372
Mol file:5401-94-5.mol

Synonyms:5-nitro-1H-indazole;5-nitroindazole

Suppliers and Price of 5-Nitroindazole

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

TRC
5-Nitroindazole
100g
$ 195.00

TRC
5-Nitroindazole
50g
$ 120.00

TCI Chemical
5-Nitroindazole >98.0%(GC)
25g
$ 53.00

SynQuest Laboratories
5-Nitro-1H-indazole 95%
100 g
$ 128.00

SynQuest Laboratories
5-Nitro-1H-indazole 95%
25 g
$ 40.00

SynQuest Laboratories
5-Nitro-1H-indazole 95%
500 g
$ 360.00

Sigma-Aldrich
5-Nitroindazole ≥99%
100g
$ 105.00

Matrix Scientific
5-Nitro-1H-indazole 99%
100g
$ 82.00

Labseeker
5-NITRO-1H-INDAZOLE 98
25g
$ 462.00

Frontier Specialty Chemicals
5-Nitroindazole 98%
25g
$ 33.00

Total 136 raw suppliers

Chemical Property of 5-Nitroindazole

Chemical Property:

Appearance/Colour:light yellow crystal
Vapor Pressure:9.79E-06mmHg at 25°C
Melting Point:207 °C
Refractive Index:1.74
Boiling Point:383.3 °C at 760 mmHg
PKA:11.71±0.40(Predicted)
Flash Point:185.6 °C
PSA：74.50000
Density:1.525 g/cm³
LogP:1.99430
Storage Temp.:Store below +30°C.
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:163.038176411
Heavy Atom Count:12
Complexity:192

Purity/Quality:

99% ^*data from raw suppliers

5-Nitroindazole ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xn, Xi
Hazard Codes:Xn,Xi
Statements: 22-36/37/38-68-36-20/21/22
Safety Statements: 26-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Nitrogen Compounds -> Other Nitrogen Rings
Canonical SMILES:C1=CC2=C(C=C1[N+](=O)[O-])C=NN2
Uses 5-Nitroindazole inhibits citrulline formation by Ca2+-calmodulin (CaM)-dependent nitric oxide synthase from bovine brain. Nitration of 5-nitroindazole with nitric acid and acetic anhydride yields 3,5-dintroindazole and 2,5-dinitroindazole.

Technology Process of 5-Nitroindazole

There total 14 articles about 5-Nitroindazole 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: 100.0%