1. Home
  2. 6-bromo-3-methoxy-1H-indazole

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

6-bromo-3-methoxy-1H-indazole

COc1n[nH]c2c1ccc(c2)Br Request for Quotation
Chemical Name: 6-bromo-3-methoxy-1H-indazole
CAS Number: 938062-38-5
Product Number: AG00602A(AGN-PC-0D5476)
Synonyms:
MDL No:
Molecular Formula: C8H7BrN2O
Molecular Weight: 227.0580

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
227.061g/mol
XLogP3:
2.5
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

Request for Quotation

Customer Feedback

Chemical Structure


6-Bromo-3-methoxy-1H-indazole is a versatile chemical compound widely utilized in chemical synthesis due to its unique properties and reactivity. This indazole derivative serves as a valuable building block in the preparation of various organic compounds and pharmaceutical intermediates. With its bromo and methoxy functional groups, 6-Bromo-3-methoxy-1H-indazole can participate in a variety of key chemical reactions, such as substitution, coupling, and cyclization reactions, making it an indispensable tool in the synthesis of complex organic molecules. Its selective reactivity makes it particularly useful in the construction of heterocyclic structures and in the modification of existing chemical entities. Additionally, the presence of the methoxy group provides opportunities for further functionalization, expanding the scope of its applications in synthetic chemistry.