Benzaldehyde, 2,3,5,6-tetrafluoro-4-hydroxy-


Chemical Name: Benzaldehyde, 2,3,5,6-tetrafluoro-4-hydroxy-
CAS Number: 24336-73-0
Product Number: AG00C1A3(AGN-PC-02NGGZ)
Synonyms:
MDL No: MFCD11505943
Molecular Formula: C7H2F4O2
Molecular Weight: 194.0832

Identification/Properties


Computed Properties
Molecular Weight:
194.085g/mol
XLogP3:
2.6
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
193.999g/mol
Monoisotopic Mass:
193.999g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
185
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



2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde is a versatile chemical compound with a wide range of applications in chemical synthesis. This compound is commonly used as a building block in the synthesis of various organic compounds due to its unique properties and reactivity. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals.One of the prominent applications of 2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde is in the synthesis of fluorinated derivatives. By utilizing its fluorine substituents, chemists can introduce fluorine atoms into organic molecules, resulting in compounds with enhanced properties such as increased stability, lipophilicity, and bioavailability. This compound is particularly valuable in the development of fluorinated pharmaceuticals, as fluorine is known to modulate the pharmacokinetic properties of drugs.Furthermore, 2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde can participate in various chemical reactions such as nucleophilic substitution, condensation, and oxidative transformations. Its hydroxy and aldehyde functional groups make it a suitable candidate for forming carbon-carbon and carbon-heteroatom bonds, allowing for the synthesis of complex molecular structures efficiently.Overall, the strategic use of 2,3,5,6-Tetrafluoro-4-hydroxybenzaldehyde in chemical synthesis enables the creation of diverse compounds with tailored properties, making it an indispensable tool for organic chemists in the development of novel materials and bioactive molecules.