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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)-

2H-Indazole, 5-bromo-2-methyl-

Brc1ccc2c(c1)cn(n2)C Request for Quotation
Chemical Name: 2H-Indazole, 5-bromo-2-methyl-
CAS Number: 465529-56-0
Product Number: AG00D80K(AGN-PC-00AN6W)
Synonyms:
MDL No:
Molecular Formula: C8H7BrN2
Molecular Weight: 211.0586

Identification/Properties

Properties
MP:
97 - 97.5 °C
BP:
322.7±15.0°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
211.062g/mol
XLogP3:
2.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
209.979g/mol
Monoisotopic Mass:
209.979g/mol
Topological Polar Surface Area:
17.8A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2H-Indazole, 5-bromo-2-methyl- is a versatile compound widely used in chemical synthesis. It serves as a key building block in the production of pharmaceuticals, agrochemicals, and materials with various applications.This derivative of indazole offers a valuable platform for the creation of novel compounds due to its unique structure and reactivity. In synthetic chemistry, it is frequently employed as a precursor for the synthesis of more complex molecules through various reactions such as substitution, addition, and coupling reactions. Its presence introduces specific functionalities into the target molecules, enhancing their properties and potential applications.Researchers and chemists utilize 2H-Indazole, 5-bromo-2-methyl- as a strategic starting material to access a diverse range of chemical structures that are not easily accessible by other means. Its incorporation in synthetic routes allows for the efficient and controlled construction of compounds with desired properties, making it an essential component in the toolbox of organic chemists.