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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)-

1H-Indazole, 5,6-dimethoxy-

COc1cc2[nH]ncc2cc1OC Request for Quotation
Chemical Name: 1H-Indazole, 5,6-dimethoxy-
CAS Number: 7746-30-7
Product Number: AG005B30(AGN-PC-02KT6R)
Synonyms:
MDL No:
Molecular Formula: C9H10N2O2
Molecular Weight: 178.1879

Identification/Properties

Properties
BP:
332.3 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H320-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


5,6-Dimethoxy-1H-indazole is a versatile compound that finds widespread application in chemical synthesis. Its unique structure and reactivity make it an essential building block in the preparation of various pharmaceuticals, agrochemicals, and materials.In chemical synthesis, 5,6-Dimethoxy-1H-indazole serves as a valuable reagent for the construction of heterocyclic frameworks. It can undergo diverse chemical transformations, such as nucleophilic substitution, electrophilic substitution, and condensation reactions, to yield a range of functionalized derivatives. Additionally, its electron-rich nature and favorable substitution patterns make it a preferred substrate for the introduction of various functional groups.One notable application of 5,6-Dimethoxy-1H-indazole is in the synthesis of bioactive molecules. By incorporating this compound into molecular scaffolds, chemists can modulate the pharmacological properties of the target compounds, such as enhancing their potency, selectivity, or metabolic stability. Moreover, the presence of methoxy groups on the indazole ring can impart desirable physicochemical properties, such as improved solubility and bioavailability, to the final products.Furthermore, 5,6-Dimethoxy-1H-indazole plays a crucial role in the synthesis of organic dyes, fluorescent probes, and materials with optical properties. Its electron-donating substituents and π-conjugated system enable the design of molecules with pronounced light-absorption and emission characteristics, making it a valuable component in the field of materials science and optoelectronics.Overall, the diverse applications of 5,6-Dimethoxy-1H-indazole in chemical synthesis highlight its significance as a key intermediate for accessing novel compounds with tailored properties and functionalities.