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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-Pyridinemethanol, 2,6-dibromo-

OCc1ccc(nc1Br)Br Request for Quotation
Chemical Name: 3-Pyridinemethanol, 2,6-dibromo-
CAS Number: 55483-88-0
Product Number: AG00E5IV(AGN-PC-0K2EB4)
Synonyms:
MDL No:
Molecular Formula: C6H5Br2NO
Molecular Weight: 266.9180

Identification/Properties

Computed Properties
Molecular Weight:
266.92g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
266.872g/mol
Monoisotopic Mass:
264.874g/mol
Topological Polar Surface Area:
33.1A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
112
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The application of (2,6-Dibromopyridin-3-yl)methanol in chemical synthesis is notable for its versatile reactivity and structural properties. As a key intermediate in organic synthesis, (2,6-Dibromopyridin-3-yl)methanol serves as a valuable building block for the construction of complex molecules and pharmaceutical compounds. Its bromopyridine moiety provides a unique reactivity profile, allowing for selective functionalization and efficient formation of new chemical bonds. Furthermore, the hydroxyl group on the methanol moiety enables diverse chemistries such as hydrogen bonding interactions and further derivatization. Overall, (2,6-Dibromopyridin-3-yl)methanol is a valuable tool for chemists engaged in the synthesis of novel compounds and materials.