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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)-

4-bromo-7-methoxy-1H-indazole

COc1ccc(c2c1[nH]nc2)Br Request for Quotation
Chemical Name: 4-bromo-7-methoxy-1H-indazole
CAS Number: 938062-01-2
Product Number: AG003KZ8(AGN-PC-0D542T)
Synonyms:
MDL No: MFCD17016112
Molecular Formula: C8H7BrN2O
Molecular Weight: 227.0580

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
227.061g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
225.974g/mol
Monoisotopic Mass:
225.974g/mol
Topological Polar Surface Area:
37.9A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
167
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


4-Bromo-7-methoxy-1H-indazole is a versatile compound that finds widespread use in chemical synthesis due to its unique properties and reactivity. In organic chemistry, this compound serves as a valuable building block for the creation of various pharmaceuticals, agrochemicals, and functional materials. When incorporated into synthesis reactions, 4-Bromo-7-methoxy-1H-indazole can act as a key intermediate, facilitating the formation of complex molecular structures.One significant application of 4-Bromo-7-methoxy-1H-indazole lies in its role as a halogen-substituted heterocycle, providing a strategic handle for diversification and functional group manipulation. The bromine atom attached to the indazole scaffold offers a site for further derivatization through various chemical transformations, enabling the introduction of different substituents or modifications to tailor the compound's properties for specific applications. Additionally, the presence of the methoxy group enhances the compound's stability and contributes to its overall reactivity profile.Furthermore, the electron-rich nature of the indazole core allows for interactions with a variety of reagents and catalysts, making 4-Bromo-7-methoxy-1H-indazole a valuable tool in the construction of biologically active molecules and other complex organic frameworks. Overall, the versatility and utility of this compound in chemical synthesis make it a valuable asset for researchers and chemists working in drug discovery, materials science, and other related fields.