66-99-9
Chemical Structure
2-Naphthaldehyde
- CAS No.: 66-99-9
- Formula:C11H8O
- Molecular Weight:156.18
IUPAC Name: 2-naphthaldehyde
InChIKey: PJKVFARRVXDXAD-UHFFFAOYSA-N
SMILES: O=CC1=CC2=C(C=CC=C2)C=C1
Biological Activity: 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
|
2-Naphthaldehyde | 99.80% | 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Naphthaldehyde (Standard) | ≥98% | 2-Naphthaldehyde (Standard) is the analytical standard of 2-Naphthaldehyde (HY-Y0075). This product is intended for research and analytical applications. 2-Naphthaldehyde is a naphthalene-based bi-aromatic aldehyde compound. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to terminate free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized to 2-naphthoic acid. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases. | ||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
|
|
2-Naphthaldehyde-13C | 2-Naphthaldehyde-13C is the 13C-labeled 2-Naphthaldehyde (HY-Y0075). 2-Naphthaldehyde belongs to naphthalene-based bis-aromatic aldehyde compounds. 2-Naphthaldehyde scavenges DPPH and ABTS+ free radicals, and exerts reductive effects by donating hydrogen atoms to interrupt free radical chain reactions. 2-Naphthaldehyde inhibits the growth and proliferation of colon cancer cells. 2-Naphthaldehyde serves as a substrate for NAD+-dependent salicylaldehyde dehydrogenase from Pseudomonas strain C6 and is catalytically oxidized. 2-Naphthaldehyde acts as a precursor material for the chemical synthesis of antioxidant Schiff bases. | |||||||||||||||||||||
|
loading...
/
|
|||||||||||||||||||||||
- [1]. Matsushita Y, et al. Antioxidant and cytotoxic activities of naphthalene derivatives from Diospyros kaki. Journal of Wood Science, 2011, 57: 161-165.
- [2]. Singh R, et al. Purification and characterization of NAD+ -dependent salicylaldehyde dehydrogenase from carbaryl-degrading Pseudomonas sp. strain C6. Applied biochemistry and biotechnology. 2014 Jan;172(2):806-19. [Content Brief]
- [3]. Oladipo SD, et al. Antidiabetes and antioxidant potential of Schiff bases derived from 2-naphthaldehye and substituted aromatic amines: Synthesis, crystal structure, Hirshfeld surface analysis, computational, and studies. Heliyon. 2024 Jan 15;10(1):e23174. [Content Brief]
