1. Home
  2. 4-bromo-1H-indazol-3-amine

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)-

4-bromo-1H-indazol-3-amine

Brc1cccc2c1c(N)n[nH]2 Request for Quotation
Chemical Name: 4-bromo-1H-indazol-3-amine
CAS Number: 914311-50-5
Product Number: AG00GRMS(AGN-PC-00J2I1)
Synonyms:
MDL No: MFCD09909580
Molecular Formula: C7H6BrN3
Molecular Weight: 212.0466

Identification/Properties

Properties
MP:
142-144°C
BP:
431.3°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
212.05g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
210.975g/mol
Monoisotopic Mass:
210.975g/mol
Topological Polar Surface Area:
54.7A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
153
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#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


4-Bromo-1H-indazol-3-amine is a versatile compound widely used in chemical synthesis as a key building block for producing various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable intermediate in the synthesis of heterocyclic compounds with diverse biological and electronic properties.In chemical synthesis, 4-Bromo-1H-indazol-3-amine serves as a starting material for the preparation of indazole derivatives, which are important scaffolds in drug discovery and development. These derivatives exhibit a wide range of biological activities, including antimicrobial, antiviral, and anticancer properties. By functionalizing the bromine group on the indazole ring, chemists can modulate the physicochemical and pharmacological properties of the resulting compounds, enhancing their efficacy and selectivity.Furthermore, 4-Bromo-1H-indazol-3-amine can be used in the synthesis of advanced materials such as organic semiconductors and dyes. Its incorporation into conjugated systems can impart desired electronic properties, making it a valuable component in the design of organic electronic devices, sensors, and optoelectronic materials.Overall, the application of 4-Bromo-1H-indazol-3-amine in chemical synthesis demonstrates its significance in drug discovery, materials science, and other fields requiring the construction of complex organic molecules with tailored properties.