CAS 34036-07-2
:3,4-Difluorobenzaldehyde
Description:
3,4-Difluorobenzaldehyde is an aromatic aldehyde characterized by the presence of two fluorine atoms positioned at the 3 and 4 positions on a benzene ring, with an aldehyde functional group (-CHO) attached. This compound typically appears as a colorless to pale yellow liquid with a distinctive aromatic odor. It is known for its reactivity due to the aldehyde group, which can participate in various chemical reactions, including nucleophilic addition and condensation reactions. The presence of fluorine atoms influences its electronic properties, making it more electrophilic compared to non-fluorinated analogs. 3,4-Difluorobenzaldehyde is used in organic synthesis and can serve as an intermediate in the production of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it exhibits moderate solubility in organic solvents, while its stability can be affected by moisture and light. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested.
Formula:C7H4F2O
InChI:InChI=1S/C7H4F2O/c8-6-2-1-5(4-10)3-7(6)9/h1-4H
InChI key:InChIKey=JPHKMYXKNKLNDF-UHFFFAOYSA-N
SMILES:C(=O)C1=CC(F)=C(F)C=C1
Synonyms:- 3,4-Difluorbenzaldehyde
- 3,4-Difluoro benzaldehyde
- 4-Amino-2-Fluorobutanoic Acid
- Benzaldehyde, 3,4-difluoro-
- Vhr Cf Df
- 3,4-Difluorobenzaldehyde
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Found 7 products.
3,4-Difluorobenzaldehyde
CAS:Formula:C7H4F2OPurity:>97.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:142.103,4-Difluorobenzaldehyde
CAS:Formula:C7H4F2OPurity:98%Color and Shape:LiquidMolecular weight:142.10293,4-Difluorobenzaldehyde
CAS:Formula:C7H4F2OPurity:≥ 98.0%Color and Shape:Colourless to pale yellow or pale orange liquidMolecular weight:142.113,4-Difluorobenzaldehyde
CAS:<p>3,4-Difluorobenzaldehyde</p>Formula:C7H4F2OPurity:96%Color and Shape: clear. colourless liquidMolecular weight:142.10g/mol3,4-Difluorobenzaldehyde
CAS:<p>3,4-Difluorobenzaldehyde is a chemical inhibitor that has been shown to be effective in the treatment of cancer. It inhibits the activity of an enzyme called tyrosine kinase by reacting with its functional group, leading to decreased production of growth factors and cell proliferation. 3,4-Difluorobenzaldehyde has been shown to have a high reaction yield in animal health studies, and it can be used as a drug for treating carcinoma cells. This compound also has strong liquid crystal properties and can be used as a component of diphenyl ether molecules. 3,4-Difluorobenzaldehyde is metabolized by the liver or excreted through urine. The pharmacokinetic properties of this compound are similar to those of other drugs that are metabolized by humans.</p>Formula:C7H4F2OPurity:Min. 95%Color and Shape:Colorless Clear LiquidMolecular weight:142.1 g/mol3,4-Difluorobenzaldehyde
CAS:<p>3,4-Difluorobenzaldehyde is a useful organic compound for research related to life sciences. The catalog number is T65937 and the CAS number is 34036-07-2.</p>Formula:C7H4F2OColor and Shape:SolidMolecular weight:142.105






