Antiseptic aldehydes

3-Hydroxy-4-methoxybenzaldehyde on condensation with furan-2-carboxylic acid hydrazide and thiophene-2-carboxylic acid hydrazide yields Schiff-bases . It undergoes condensation reaction with1-azabicyclo[2.

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

3-Methylpyridine-2-carboxaldehyde

Application 3-Phenylbutyraldehyde was used as a reactant to study the kinetics of the reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G .

Application 3-Phenylbutyraldehyde was used as a reactant to study the kinetics of the reaction of hydrogen peroxide and certain aromatic aldehydes with cytochrome P450BM3-F87G .

Analysis Note Assay (GC, area%): &#8805 95.0 % (a/a) Density (d 20&#8199&#176C/ 4&#8199&#176C): 1.

3- tert -Butyl-2-hydroxybenzaldehyde is a mono- tert -butyl substituted 2-hydroxybenzaldehyde that can be synthesized using ethylbromide and 2 -tert -butylphenol. Application 3- tert -Butyl-2-hydroxybenzaldehyde may be used in the synthesis of:

3- tert -Butyl-2-hydroxybenzaldehyde is a mono- tert -butyl substituted 2-hydroxybenzaldehyde that can be synthesized using ethylbromide and 2 -tert -butylphenol. Application 3- tert -Butyl-2-hydroxybenzaldehyde may be used in the synthesis of:

3-Vinylbenzaldehyde (3-VBAL) contains a vinyl group bonded to the aromatic ring of benzaldehyde. Pulsed plasma polymerization of 3-VBAL has been described.

2,6-Dimethyl-4-pyrrone has been reported to undergo photochemical rearrangement to afford 4,5-dimethyl-2-furaldehyde. Mechanism of this photorearrangement has been described.

2,6-Dimethyl-4-pyrrone has been reported to undergo photochemical rearrangement to afford 4,5-dimethyl-2-furaldehyde. Mechanism of this photorearrangement has been described.

Application AIE (aggregation-induced emission)-active building block.