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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-methoxy-

COc1ccc2c(c1)cn[nH]2 Request for Quotation
Chemical Name: 1H-Indazole, 5-methoxy-
CAS Number: 94444-96-9
Product Number: AG003MTS(AGN-PC-00M64O)
Synonyms:
MDL No: MFCD07781657
Molecular Formula: C8H8N2O
Molecular Weight: 148.1619

Identification/Properties

Properties
BP:
312.5°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
148.165g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
148.064g/mol
Monoisotopic Mass:
148.064g/mol
Topological Polar Surface Area:
37.9A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methoxy-1H-indazole is a versatile compound widely utilized in chemical synthesis as a key building block for the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. With its unique structure and reactivity, this indazole derivative serves as an essential intermediate in the production of diverse compounds with significant commercial and scientific applications.In the realm of medicinal chemistry, 5-Methoxy-1H-indazole plays a crucial role in the development of novel drug candidates targeting a wide range of biological mechanisms. Its structural features make it valuable for designing molecules with potential therapeutic activities, such as anticancer agents, antimicrobial drugs, and central nervous system (CNS) modulators. By incorporating 5-Methoxy-1H-indazole into synthetic routes, researchers can access a multitude of derivatives with varying pharmacological properties, enabling the discovery of new lead compounds for the treatment of various diseases.Furthermore, in the field of agrochemicals, the strategic use of 5-Methoxy-1H-indazole has led to the synthesis of innovative pesticides, herbicides, and fungicides that exhibit enhanced efficacy and selectivity. By harnessing the chemical reactivity of this indazole derivative, scientists can tailor the properties of agricultural chemicals to address specific pest or weed control requirements, thereby contributing to sustainable farming practices and crop protection.Overall, the versatility of 5-Methoxy-1H-indazole in chemical synthesis underscores its significance as a valuable building block in the creation of diverse molecules with important applications in medicine, agriculture, and beyond. Its strategic incorporation into synthetic pathways opens up avenues for the development of new and improved chemical entities that hold the potential to address pressing societal needs and advance scientific knowledge in various fields.