CAS 3453-33-6
:6-Methoxy-2-naphthaldehyde
Description:
6-Methoxy-2-naphthaldehyde is an organic compound characterized by its naphthalene structure with a methoxy group and an aldehyde functional group. It features a methoxy (-OCH₃) substituent at the 6-position and an aldehyde (-CHO) at the 2-position of the naphthalene ring. This compound typically appears as a yellow to light brown solid and is known for its aromatic properties, which contribute to its potential applications in organic synthesis and as a building block in the development of various chemical compounds. It is soluble in organic solvents such as ethanol and dichloromethane but has limited solubility in water. The presence of both the methoxy and aldehyde groups allows for various chemical reactivity, including electrophilic aromatic substitution and condensation reactions. Additionally, 6-Methoxy-2-naphthaldehyde may exhibit biological activity, making it of interest in medicinal chemistry and material science. Safety precautions should be taken when handling this compound, as with many organic chemicals, due to potential toxicity and reactivity.
Formula:C12H10O2
InChI:InChI=1/C12H10O2/c1-14-12-5-4-10-6-9(8-13)2-3-11(10)7-12/h2-8H,1H3
InChI key:InChIKey=VZBLASFLFFMMCM-UHFFFAOYSA-N
SMILES:C(=O)C1=CC2=C(C=C(OC)C=C2)C=C1
Synonyms:- 2-Formyl-6-methoxynaphthalene
- 2-Methoxy-6-naphthaldehyde
- 2-Methoxy-6-naphthalenecarboxaldehyde
- 2-Naphthaldehyde, 6-methoxy-
- 2-Naphthalenecarboxaldehyde, 6-methoxy-
- 6-Methoxy-2-Naphtaldehyde
- 6-Methoxy-2-Naphthalaldehyde
- 6-Methoxy-2-naphthaldehyde,99%
- 6-Methoxy-2-naphthalenecarboxaldehyde
- 6-Methoxynaphthalene-2-Carbaldehyde
- Asinex-Reag Bas 07663025
- Labotest-Bb Lt01147524
- Monal 62
- Timtec-Bb Sbb010060
- 6-Methoxy-2-naphthaldehyde
- 6-Methoxy-2-naphthaldehyde ,98%
- 6-METHOXY-2-NAPHTHALDEHYDENABUMETONE
- See more synonyms
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Found 10 products.
6-Methoxy-2-naphthaldehyde
CAS:Formula:C12H10O2Purity:>97.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:186.216-Methoxy-2-naphthaldehyde, 99%
CAS:<p>6-Methoxy-2-naphthaldehyde is used as a diagnostic reagent in tumor studies involving aldehyde dehydrogenase enzymes. In addition it is used in organic synthesis reactions forming fluorescent substrates for inhibition studies relating to hypertension and vascular inflammation. It is also used as int</p>Formula:C12H10O2Purity:99%Color and Shape:Crystals or powder or crystalline powder, White to yellow to orangeMolecular weight:186.216-Methoxy-2-Naphthaldehyde
CAS:Formula:C12H10O2Purity:95%Color and Shape:SolidMolecular weight:186.20666-Methoxy-2-naphthaldehyde
CAS:6-Methoxy-2-naphthaldehydeFormula:C12H10O2Purity:98%Color and Shape: faint to light brown powderMolecular weight:186.21g/mol6-Methoxy-2-naphthalenecarboxaldehyde
CAS:Controlled ProductFormula:C12H10O2Color and Shape:NeatMolecular weight:186.216-Methoxy-2-naphthaldehyde
CAS:<p>6-Methoxy-2-naphthaldehyde is a nonsteroidal antiinflammatory drug that belongs to the class of naphthalenes. It inhibits the formation of inflammatory prostaglandins, which are mediators of pain and inflammation. 6-Methoxy-2-naphthaldehyde has been shown to have cytotoxic effects on cancer cells and in vitro studies have shown that it can induce cell lysis. It has also been shown to be a potent fluorescence probe for use in biological applications. This compound binds to human serum proteins by hydrogen bonding interactions, which may affect its pharmacokinetic properties. In addition, this compound has been shown to inhibit the activity of detoxification enzymes such as CYP 2C9 and 2D6 at high concentrations, which may lead to unwanted side effects such as nausea or vomiting. The molecular docking analysis of 6-Methoxy-2-naphthaldehyde with the active site of human liver alcohol dehydrogen</p>Formula:C12H10O2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:186.21 g/mol6-Methoxy-2-naphthaldehyde
CAS:Formula:C12H10O2Purity:95%Color and Shape:SolidMolecular weight:186.21









