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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-Pyridinol, 5-bromo-2-methyl-

Brc1cnc(c(c1)O)C Request for Quotation
Chemical Name: 3-Pyridinol, 5-bromo-2-methyl-
CAS Number: 91420-25-6
Product Number: AG00H0XR(AGN-PC-00LKRG)
Synonyms:
MDL No:
Molecular Formula: C6H6BrNO
Molecular Weight: 188.0219

Identification/Properties

Properties
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
188.024g/mol
XLogP3:
1.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
186.963g/mol
Monoisotopic Mass:
186.963g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99.1
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-methylpyridin-3-ol, also known as $name$, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in organic reactions, particularly in the production of pharmaceuticals, agrochemicals, and advanced materials.One of the primary applications of 5-Bromo-2-methylpyridin-3-ol in chemical synthesis is as a key building block in the synthesis of heterocyclic compounds. Its unique structure and reactivity make it an essential precursor in the preparation of various pharmaceutical agents, such as anti-inflammatory drugs and antiviral medications. By serving as a foundational component, this compound enables the efficient synthesis of complex molecules with specific biological activities.Moreover, 5-Bromo-2-methylpyridin-3-ol is often employed in transition metal-catalyzed reactions to facilitate the creation of new carbon-carbon and carbon-heteroatom bonds. This compound's functional groups enable selective derivatization, allowing for the modification of molecular structures to achieve desired properties. Its versatility and compatibility with various synthetic methodologies make it a valuable tool for chemists in designing and constructing novel chemical entities for diverse applications.Overall, the strategic incorporation of 5-Bromo-2-methylpyridin-3-ol in chemical synthesis enables the efficient and targeted production of functionalized molecules with potential therapeutic, agricultural, and material science applications.