(5-methoxypyridin-3-yl)methanol


Chemical Name: (5-methoxypyridin-3-yl)methanol
CAS Number: 937202-11-4
Product Number: AG00GX5V(AGN-PC-07CGHP)
Synonyms:
MDL No:
Molecular Formula: C7H9NO2
Molecular Weight: 139.1519

Identification/Properties


Computed Properties
Molecular Weight:
139.154g/mol
XLogP3:
-0.1
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#:
-
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum


Other Analytical Data


Request for Quotation


Customer Feedback


Chemical Structure



The compound we offer, (5-Methoxypyridin-3-yl)methanol, plays a crucial role in various chemical synthesis applications. Its unique structure and properties make it a valuable reagent in organic chemistry research and production processes. With its functional group, this compound serves as a versatile building block for the synthesis of diverse organic molecules, including pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, (5-Methoxypyridin-3-yl)methanol can be utilized as a key intermediate for introducing specific functional groups or modifying molecular structures. Its reactivity allows for the creation of complex compounds with tailored properties, facilitating the development of new materials and bioactive molecules. Additionally, this compound can participate in various organic transformations such as oxidation, reduction, and substitution reactions, enabling the efficient construction of intricate chemical architectures.Furthermore, (5-Methoxypyridin-3-yl)methanol offers chemists the flexibility to design and construct molecular scaffolds with precise control over stereochemistry and regioselectivity. Its strategic incorporation into synthetic pathways enhances the efficiency and selectivity of processes, leading to the synthesis of target compounds with improved yields and purity. Overall, the utility of this compound in chemical synthesis underscores its significance as a valuable tool for advancing research and innovation in the field of organic chemistry.