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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,7-bromo-3-chloro-

Brc1cccc2c1[nH]nc2Cl Request for Quotation
Chemical Name: 1H-Indazole,7-bromo-3-chloro-
CAS Number: 885271-75-0
Product Number: AG0046XX(AGN-PC-0VM564)
Synonyms:
MDL No:
Molecular Formula: C7H4BrClN2
Molecular Weight: 231.4771

Identification/Properties

Properties
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
231.477g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
229.925g/mol
Monoisotopic Mass:
229.925g/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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


7-Bromo-3-chloro-1H-indazole is a versatile building block in chemical synthesis, commonly used in pharmaceutical and agrochemical industries. This compound serves as an important intermediate for the synthesis of various biologically active molecules. Its unique structure offers opportunities for diversification through functional group modifications, making it a valuable tool for creating new compounds with desired pharmacological properties. In particular, 7-Bromo-3-chloro-1H-indazole is frequently employed in the synthesis of heterocyclic compounds, such as indazoles and indazolones, which are known for their diverse biological activities. Furthermore, its halogen substituents can facilitate further transformations, enabling the preparation of structurally complex and diverse compounds for various applications in drug discovery and chemical research.