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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)-

2-Pyridinemethanol, 5-methoxy-

COc1ccc(nc1)CO Request for Quotation
Chemical Name: 2-Pyridinemethanol, 5-methoxy-
CAS Number: 127978-70-5
Product Number: AG000XML(AGN-PC-0NI3YZ)
Synonyms:
MDL No:
Molecular Formula: C7H9NO2
Molecular Weight: 139.1519

Identification/Properties

Computed Properties
Molecular Weight:
139.154g/mol
XLogP3:
0
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
139.063g/mol
Monoisotopic Mass:
139.063g/mol
Topological Polar Surface Area:
42.4A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
97.6
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-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Methoxypyridine-2-yl)methanol is a versatile compound commonly used in chemical synthesis. Its primary application lies in its ability to function as a valuable building block in the creation of various pharmaceuticals and agrochemicals. By incorporating 5-Methoxypyridine-2-yl)methanol into synthesis strategies, chemists can access a wide range of functionalized molecules with diverse properties and applications. Additionally, this compound demonstrates reactivity with various reagents, allowing for the development of innovative synthetic routes and the preparation of complex molecular structures. In summary, the utilization of (5-Methoxypyridine-2-yl)methanol in chemical synthesis offers a powerful tool for the design and production of novel compounds with potential benefits across different industries.