Benzaldehyde, 2-methoxy-5-(trifluoromethyl)-


Chemical Name: Benzaldehyde, 2-methoxy-5-(trifluoromethyl)-
CAS Number: 146539-83-5
Product Number: AG001E43(AGN-PC-0KKZGB)
Synonyms:
MDL No:
Molecular Formula: C9H7F3O2
Molecular Weight: 204.1459

Identification/Properties


Properties
MP:
85-89 °C
BP:
237.5°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Stability:
Air Sensitive
Computed Properties
Molecular Weight:
204.148g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
204.04g/mol
Monoisotopic Mass:
204.04g/mol
Topological Polar Surface Area:
26.3A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
203
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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NMR Spectrum


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Chemical Structure



2-Methoxy-5-(trifluoromethyl)benzaldehyde, also known as $name$, is a versatile chemical compound widely utilized in various chemical synthesis applications. This compound plays a crucial role as a key building block in the production of pharmaceuticals, agrochemicals, and advanced materials.In chemical synthesis, 2-Methoxy-5-(trifluoromethyl)benzaldehyde serves as a valuable intermediate for the synthesis of diverse compounds due to its unique structural properties. It acts as a precursor in the preparation of complex molecules with specific functionalities, making it an essential component in the development of new materials and substances.Additionally, this compound is commonly employed in the synthesis of heterocyclic compounds, which are vital in the pharmaceutical industry for the design and production of various drugs. Its ability to undergo reactions such as condensation, oxidation, and reduction makes it a versatile and indispensable reagent in organic synthesis.Furthermore, the trifluoromethyl group in 2-Methoxy-5-(trifluoromethyl)benzaldehyde imparts desirable characteristics to the molecules it is incorporated into, enhancing their biological activity and chemical stability. This property makes it particularly valuable in medicinal chemistry for the creation of bioactive compounds with enhanced properties.Overall, 2-Methoxy-5-(trifluoromethyl)benzaldehyde plays a crucial role in chemical synthesis by enabling the efficient and precise construction of complex molecules for a wide range of industrial applications. Its versatility and unique chemical properties make it an indispensable tool for synthetic chemists striving to develop innovative materials and compounds.