1. Home
  2. 2H-Indazole, 2,3-dimethyl-6-nitro-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2H-Indazole, 2,3-dimethyl-6-nitro-

[O-][N+](=O)c1ccc2c(c1)nn(c2C)C Request for Quotation
Chemical Name: 2H-Indazole, 2,3-dimethyl-6-nitro-
CAS Number: 444731-73-1
Product Number: AG0032Y5(AGN-PC-0N4W8E)
Synonyms:
MDL No:
Molecular Formula: C9H9N3O2
Molecular Weight: 191.1867

Identification/Properties

Properties
MP:
183-186°C
BP:
377°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
191.19g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
191.069g/mol
Monoisotopic Mass:
191.069g/mol
Topological Polar Surface Area:
63.6A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
241
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,3-Dimethyl-6-nitro-2H-indazole is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as a valuable building block in the formation of various complex organic molecules. Its nitro group can undergo multiple chemical reactions, such as reduction or substitution, to yield a range of functionalized derivatives. In addition, the methyl groups at positions 2 and 3 contribute to the compound's stability and can influence its reactivity during synthetic processes. Overall, 2,3-Dimethyl-6-nitro-2H-indazole plays a crucial role in the creation of diverse chemical structures in the field of organic synthesis.