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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)-

2,3-dimethylindazol-6-amine;hydrochloride

Nc1ccc2c(c1)nn(c2C)C.Cl Request for Quotation
Chemical Name: 2,3-dimethylindazol-6-amine;hydrochloride
CAS Number: 635702-60-2
Product Number: AG00IB8J(AGN-PC-07ZXB1)
Synonyms:
MDL No: MFCD17014819
Molecular Formula: C9H12ClN3
Molecular Weight: 197.6647

Identification/Properties

Properties
MP:
>230°C (dec.)
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
197.666g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
197.072g/mol
Monoisotopic Mass:
197.072g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
171
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:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,3-Dimethyl-2H-indazol-6-amine hydrochloride is a versatile compound widely used in chemical synthesis. With its unique structure and reactivity, this compound serves as a valuable building block for the creation of various organic molecules. In particular, it is commonly employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.Due to its specific chemical properties, 2,3-Dimethyl-2H-indazol-6-amine hydrochloride can participate in a range of important reactions such as substitutions, additions, and condensations. This enables chemists to efficiently introduce functional groups or modify existing molecules to achieve desired properties. Additionally, the presence of the amine group in this compound allows for further derivatization, expanding its utility in diverse synthetic pathways.Moreover, the incorporation of 2,3-Dimethyl-2H-indazol-6-amine hydrochloride into complex molecules can lead to the development of new compounds with potential biological activities or industrial applications. Its use in chemical synthesis facilitates the production of innovative intermediates and final products, contributing to advancements in drug discovery, material science, and other fields.