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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-bromo-7-iodo-

Brc1cc(I)c2c(c1)cn[nH]2 Request for Quotation
Chemical Name: 1H-Indazole, 5-bromo-7-iodo-
CAS Number: 953410-86-1
Product Number: AG005S4P(AGN-PC-0CPH4Q)
Synonyms:
MDL No:
Molecular Formula: C7H4BrIN2
Molecular Weight: 322.9285

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
322.931g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
321.86g/mol
Monoisotopic Mass:
321.86g/mol
Topological Polar Surface Area:
28.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
155
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

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-7-iodo-1H-indazole is a versatile compound widely used in chemical synthesis for its unique reactivity and functional properties. This compound serves as a valuable building block in the creation of complex organic molecules and pharmaceutical intermediates. Its strategic placement of bromine and iodine atoms allows for selective transformations in various synthetic routes. In particular, 5-Bromo-7-iodo-1H-indazole is utilized in the synthesis of heterocyclic compounds, coordination complexes, and bioactive molecules. Its compatibility with a wide range of reaction conditions and its ability to undergo diverse chemical transformations make it a valuable tool for researchers and chemists in the pharmaceutical, agrochemical, and material science industries. Through its incorporation into synthetic pathways, 5-Bromo-7-iodo-1H-indazole enables the efficient construction of novel compounds with potential applications in drug discovery and material design.