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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)-

(5-(Benzyloxy)-6-chloro-4-iodopyridin-2-yl)methanol

OCc1cc(I)c(c(n1)Cl)OCc1ccccc1 Request for Quotation
Chemical Name: (5-(Benzyloxy)-6-chloro-4-iodopyridin-2-yl)methanol
CAS Number: 1186405-17-3
Product Number: AG009KNN(AGN-PC-0WAG8W)
Synonyms:
MDL No:
Molecular Formula: C13H11ClINO2
Molecular Weight: 375.5894

Identification/Properties

Computed Properties
Molecular Weight:
375.59g/mol
XLogP3:
3.1
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
374.952g/mol
Monoisotopic Mass:
374.952g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
18
Formal Charge:
0
Complexity:
251
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


The compound (5-(Benzyloxy)-6-chloro-4-iodopyridin-2-yl)methanol, commonly referred to as $name$, serves as a versatile building block in organic synthesis. Its unique molecular structure allows for a range of chemical transformations to be carried out, making it a valuable tool for chemists in the laboratory.One key application of $name$ lies in its role as a precursor for the synthesis of various heterocyclic compounds. By utilizing the functional groups present in this molecule, chemists can selectively modify the aromatic ring and introduce new substituents at specific positions. This capability enables the creation of structurally diverse molecules with tailored properties, making it ideal for medicinal chemistry and drug development.Furthermore, the presence of both chlorine and iodine atoms in $name$ imparts reactivity that can be harnessed in cross-coupling reactions. These reactions allow for the formation of new carbon-carbon or carbon-heteroatom bonds, expanding the synthetic possibilities afforded by this compound. By leveraging the reactivity of $name$ in these coupling reactions, chemists can access complex molecular frameworks with high efficiency.In summary, (5-(Benzyloxy)-6-chloro-4-iodopyridin-2-yl)methanol, or $name$, is a valuable tool in chemical synthesis, offering versatility and reactivity that enable the construction of diverse organic molecules. Its application in the synthesis of heterocycles and its utility in cross-coupling reactions highlight its importance in modern organic chemistry research.