1-Naphthalenol, 6-methoxy-


Chemical Name: 1-Naphthalenol, 6-methoxy-
CAS Number: 22604-07-5
Product Number: AG006X9A(AGN-PC-0NECOJ)
Synonyms:
MDL No:
Molecular Formula: C11H10O2
Molecular Weight: 174.1959

Identification/Properties


Computed Properties
Molecular Weight:
174.199g/mol
XLogP3:
3.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
174.068g/mol
Monoisotopic Mass:
174.068g/mol
Topological Polar Surface Area:
29.5A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
170
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

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Chemical Structure



6-Methoxynaphthalen-1-ol, also known as MNOL, is a versatile compound widely utilized in chemical synthesis. This compound plays a crucial role in organic chemistry as a key building block in the production of various pharmaceuticals, agrochemicals, and specialty chemicals. MNOL is particularly valued for its ability to serve as a precursor in the synthesis of different functionalized naphthalene derivatives.In chemical synthesis, 6-Methoxynaphthalen-1-ol is frequently employed as a starting material for the preparation of specialized molecules with unique properties. By incorporating MNOL into a synthesis route, chemists can introduce a methoxy group at a specific position on the naphthalene ring, enabling precise control over the structural characteristics and functional groups present in the final compound. This level of structural manipulation is crucial in the design and development of new chemical entities with desired bioactivities or physical properties.Furthermore, the reactivity of the hydroxyl group in MNOL allows for further derivatization through various chemical reactions, including acylation, alkylation, and reduction, expanding the range of potential applications in organic synthesis. By functionalizing MNOL with different substituents, researchers can tailor the compound's properties to meet specific requirements for a wide range of industrial and scientific purposes.Overall, 6-Methoxynaphthalen-1-ol serves as a valuable tool in chemical synthesis, enabling scientists to access a diverse array of functionalized naphthalene derivatives with tailored properties and applications across multiple sectors, including pharmaceuticals, materials science, and agrochemicals.