Benzaldehyde, 2-(3-methoxyphenoxy)-


Chemical Name: Benzaldehyde, 2-(3-methoxyphenoxy)-
CAS Number: 122283-23-2
Product Number: AG001722(AGN-PC-001ZPY)
Synonyms:
MDL No:
Molecular Formula: C14H12O3
Molecular Weight: 228.2433

Identification/Properties


Properties
MP:
34-38℃
Form:
Solid
Computed Properties
Molecular Weight:
228.247g/mol
XLogP3:
3.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
228.079g/mol
Monoisotopic Mass:
228.079g/mol
Topological Polar Surface Area:
35.5A^2
Heavy Atom Count:
17
Formal Charge:
0
Complexity:
242
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:
Danger
UN#:
3077
Hazard Statements:
H318-H400
Precautionary Statements:
P273-P280-P305+P351+P338
Class:
9
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-(3-Methoxyphenoxy)benzaldehyde, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a crucial building block in the creation of various organic compounds, particularly in the realm of pharmaceuticals and fine chemicals. Due to its unique chemical structure, 2-(3-Methoxyphenoxy)benzaldehyde offers a range of functionalities that make it an essential reagent in modern organic synthesis.One key application of 2-(3-Methoxyphenoxy)benzaldehyde is its role as a precursor in the synthesis of heterocyclic compounds. By reacting with different nucleophiles or electrophiles, this compound can be utilized to form a diverse array of heterocycles, such as benzofurans, benzothiazoles, and benzoxazoles. These heterocyclic compounds are crucial in the development of new drugs, agrochemicals, and materials with specialized properties.Furthermore, 2-(3-Methoxyphenoxy)benzaldehyde is commonly employed in the preparation of various aromatic derivatives through alkylation, acylation, or condensation reactions. Its aromatic aldehyde group provides a reactive site for functionalization, enabling chemists to introduce different substituents and modify the compound's properties according to the desired application. This versatility makes 2-(3-Methoxyphenoxy)benzaldehyde a valuable tool in the design and synthesis of complex organic molecules.Overall, the strategic incorporation of 2-(3-Methoxyphenoxy)benzaldehyde in chemical synthesis offers a pathway to access diverse chemical structures and functional groups, making it an indispensable component in the development of advanced materials, pharmaceuticals, and agrochemicals.