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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)-

3-Bromo-1-methyl-1H-indazol-5-ylamine

Nc1ccc2c(c1)c(Br)nn2C Request for Quotation
Chemical Name: 3-Bromo-1-methyl-1H-indazol-5-ylamine
CAS Number: 1092351-49-9
Product Number: AG008S3L(AGN-PC-05SPJP)
Synonyms:
MDL No:
Molecular Formula: C8H8BrN3
Molecular Weight: 226.0732

Identification/Properties

Computed Properties
Molecular Weight:
226.077g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
224.99g/mol
Monoisotopic Mass:
224.99g/mol
Topological Polar Surface Area:
43.8A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
176
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


3-Bromo-1-methyl-1H-indazol-5-amine, also known as $name$, is a versatile compound widely used in chemical synthesis processes. This compound plays a crucial role in the development of pharmaceuticals, agrochemicals, and advanced materials due to its unique chemical properties.In chemical synthesis, 3-Bromo-1-methyl-1H-indazol-5-amine serves as a valuable building block for the creation of various organic molecules. Its bromine and amine functional groups make it an ideal candidate for coupling reactions, such as Suzuki-Miyaura cross-coupling and Buchwald-Hartwig amination. These reactions allow for the efficient formation of complex molecular structures with high precision.Furthermore, 3-Bromo-1-methyl-1H-indazol-5-amine can be selectively functionalized at the indazole nitrogen or methyl group, enabling the synthesis of diverse derivatives with tailored properties. This versatility opens up opportunities for the design and development of novel compounds with potential applications in drug discovery, materials science, and crop protection.Overall, the use of 3-Bromo-1-methyl-1H-indazol-5-amine in chemical synthesis offers researchers a powerful tool to access structurally diverse compounds with a wide range of applications. Its importance in the field of organic chemistry cannot be understated, making it a valuable component in the toolbox of synthetic chemists seeking to create innovative molecules for various industries.