Cas no 1214358-05-0 (4-(Difluoromethoxy)-2-fluorobenzaldehyde)

4-(Difluoromethoxy)-2-fluorobenzaldehyde is a fluorinated aromatic aldehyde characterized by its difluoromethoxy and fluorine substituents, which enhance its reactivity and stability in synthetic applications. The presence of electron-withdrawing groups makes it a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly for constructing complex heterocycles or fluorinated compounds. Its high purity and well-defined structure ensure consistent performance in cross-coupling reactions, nucleophilic additions, and other transformations. The compound's stability under typical reaction conditions allows for versatile use in multi-step syntheses. Suitable for research and industrial applications, it offers precise control in the development of fluorinated target molecules.
4-(Difluoromethoxy)-2-fluorobenzaldehyde structure
1214358-05-0 structure
Product Name:4-(Difluoromethoxy)-2-fluorobenzaldehyde
CAS No:1214358-05-0
MF:C8H5F3O2
MW:190.119313001633
MDL:MFCD11847162
CID:830623
PubChem ID:46311636
Update Time:2025-05-22

4-(Difluoromethoxy)-2-fluorobenzaldehyde Chemical and Physical Properties

Names and Identifiers

    • 4-(Difluoromethoxy)-2-fluorobenzaldehyde
    • DTXSID70673306
    • YYCQRWDSMUIVEY-UHFFFAOYSA-N
    • CL8348
    • EN300-364732
    • 1214358-05-0
    • SY212093
    • Benzaldehyde, 4-(difluoromethoxy)-2-fluoro-
    • AS-46018
    • CS-0455172
    • Z1255439533
    • 4-Difluoromethoxy-2-fluorobenzaldehyde
    • MFCD11847162
    • SCHEMBL16742810
    • DB-349192
    • AKOS015999933
    • MDL: MFCD11847162
    • Inchi: 1S/C8H5F3O2/c9-7-3-6(13-8(10)11)2-1-5(7)4-12/h1-4,8H
    • InChI Key: YYCQRWDSMUIVEY-UHFFFAOYSA-N
    • SMILES: FC1C=C(C=CC=1C=O)OC(F)F

Computed Properties

  • Exact Mass: 190.02416388g/mol
  • Monoisotopic Mass: 190.02416388g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 3
  • Complexity: 175
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 2.4
  • Topological Polar Surface Area: 26.3?2

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4-(Difluoromethoxy)-2-fluorobenzaldehyde Related Literature

Additional information on 4-(Difluoromethoxy)-2-fluorobenzaldehyde

Comprehensive Overview of 4-(Difluoromethoxy)-2-fluorobenzaldehyde (CAS No. 1214358-05-0)

4-(Difluoromethoxy)-2-fluorobenzaldehyde (CAS No. 1214358-05-0) is a fluorinated aromatic aldehyde with significant applications in pharmaceutical and agrochemical research. This compound, characterized by its difluoromethoxy and fluoro substituents, has garnered attention due to its unique chemical properties and versatility in synthetic chemistry. Researchers and industry professionals frequently search for terms like "4-(Difluoromethoxy)-2-fluorobenzaldehyde synthesis", "CAS 1214358-05-0 applications", and "fluorinated benzaldehyde derivatives", reflecting its relevance in modern chemical innovation.

The molecular structure of 4-(Difluoromethoxy)-2-fluorobenzaldehyde features a benzaldehyde core substituted with a difluoromethoxy group at the 4-position and a fluorine atom at the 2-position. This arrangement enhances its reactivity and stability, making it a valuable intermediate in the synthesis of complex molecules. Recent trends in green chemistry and sustainable synthesis have spurred interest in optimizing its production methods, with queries such as "eco-friendly synthesis of fluorinated aldehydes" gaining traction in academic and industrial circles.

In pharmaceutical research, 4-(Difluoromethoxy)-2-fluorobenzaldehyde serves as a key building block for drug candidates targeting central nervous system (CNS) disorders and metabolic diseases. Its fluorine-rich structure improves bioavailability and metabolic stability, addressing common challenges in drug development. Searches like "fluorinated aldehydes in drug design" and "CAS 1214358-05-0 in medicinal chemistry" highlight its growing role in this field. Additionally, its potential in agrochemical formulations has been explored, particularly in developing pesticides and herbicides with enhanced efficacy.

The compound's physicochemical properties, such as its melting point, solubility, and reactivity, are critical for its application in various reactions. Analytical techniques like NMR spectroscopy and HPLC are commonly employed to characterize and purify 4-(Difluoromethoxy)-2-fluorobenzaldehyde. Queries such as "analytical methods for fluorobenzaldehydes" and "CAS 1214358-05-0 purity standards" reflect the demand for precise quality control in its usage.

From a commercial perspective, 4-(Difluoromethoxy)-2-fluorobenzaldehyde is supplied by specialized chemical manufacturers catering to research institutions and pharmaceutical companies. Its market demand is driven by the increasing focus on fluorine-containing compounds in life sciences. Search terms like "suppliers of CAS 1214358-05-0" and "bulk purchase of fluorinated benzaldehydes" indicate its economic significance. Regulatory compliance and safety data are also frequently searched topics, emphasizing the need for transparent handling guidelines.

Future research directions for 4-(Difluoromethoxy)-2-fluorobenzaldehyde may include exploring its role in catalysis and material science, particularly in designing advanced polymers and electronic materials. The compound's adaptability aligns with emerging trends in high-performance materials and nanotechnology. As the scientific community continues to investigate its potential, queries like "innovative uses of fluorinated aldehydes" and "CAS 1214358-05-0 in nanotechnology" are expected to rise.

In summary, 4-(Difluoromethoxy)-2-fluorobenzaldehyde (CAS No. 1214358-05-0) is a multifaceted compound with broad applications in pharmaceuticals, agrochemicals, and material science. Its unique structural features and reactivity make it a subject of ongoing research and industrial interest. By addressing common search queries and aligning with contemporary scientific trends, this overview underscores the compound's importance in modern chemistry.

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