66-99-9
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 is an aromatic aldehyde. 2-Naphthaldehyde is soluble in various organic solvents. 2-Naphthaldehyde can participate in chemical reactions to generate functionalized ketone derivatives[1][2].
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2-Naphthaldehyde | 99.80% | 2-Naphthaldehyde is an aromatic aldehyde. 2-Naphthaldehyde is soluble in various organic solvents. 2-Naphthaldehyde can participate in chemical reactions to generate functionalized ketone derivatives. | ||||||||||||||||||||
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2-Naphthaldehyde (Standard) | ≥98% | 2-Naphthaldehyde is an aromatic aldehyde. 2-Naphthaldehyde is soluble in various organic solvents. 2-Naphthaldehyde can participate in chemical reactions to generate functionalized ketone derivatives. | ||||||||||||||||||||
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2-Naphthaldehyde-13C | 2-Naphthaldehyde-13C is the 13C-labeled 2-Naphthaldehyde (HY-Y0075). 2-Naphthaldehyde is an aromatic aldehyde. 2-Naphthaldehyde is soluble in various organic solvents. 2-Naphthaldehyde can participate in chemical reactions to generate functionalized ketone derivatives. | |||||||||||||||||||||
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References
- [1]. Zhang F, et al. Solubility measurement and correlation for 2-naphthaldehyde in pure organic solvents and methanol+ ethanol mixtures[J]. Journal of Chemical & Engineering Data, 2015, 60(8): 2502-2509.
- [2]. Ishii T, et al. N-Heterocyclic Carbene-Catalyzed Radical Relay Enabling Vicinal Alkylacylation of Alkenes. J Am Chem Soc. 2019 Sep 11;141(36):14073-14077. [Content Brief]
