CAS 158365-55-0
:1-Naphthalenecarboxaldehyde,7-methoxy-
Description:
1-Naphthalenecarboxaldehyde, 7-methoxy- is an organic compound characterized by its naphthalene backbone, which features a methoxy group (-OCH3) and an aldehyde functional group (-CHO) at specific positions on the aromatic ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and temperature. It is known for its aromatic properties and is often used in organic synthesis and as an intermediate in the production of various chemical compounds. The presence of the methoxy group can influence its reactivity and solubility, making it more polar compared to its parent naphthalene structure. Additionally, 1-Naphthalenecarboxaldehyde, 7-methoxy- may exhibit biological activity, which can be of interest in medicinal chemistry. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure proper safety measures are taken due to potential hazards associated with its use.
Formula:C12H10O2
Synonyms:- 7-Methoxy-1-naphthaldehyde
- 7-Methoxy-1-naphthalenecarboxaldehyde
- Monal 71
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 5 products.
7-METHOXYNAPHTHALENE-1-CARBOXALDEHYDE
CAS:Formula:C12H10O2Purity:97%Color and Shape:SolidMolecular weight:186.20667-Methoxy-1-naphthaldehyde
CAS:Controlled Product<p>Applications One of the two highly fluorogenic aldehydes, 7-Methoxy-1-naphthaldehyde (MONAL-71) and 6-Methoxy-2-naphthaldehyde (MONAL-62), as indicators of the aldehyde dehydrogenase (ALDH) activity in human tissue homogenates and accessible body fluids.This compound is suitable for aldehyde dehydrogenase (ALDH) related research.<br>References Wierzchowski, J., et al.: Anal. Biochem., 245, 69 (1997),<br></p>Formula:C12H10O2Color and Shape:NeatMolecular weight:186.2077-Methoxy-1-naphthaldehyde
CAS:<p>7-Methoxy-1-naphthaldehyde is an aldehyde that is synthesized from acetaldehyde and 7-methoxy-1-naphthol. It has been shown to inhibit the cytosolic aldehyde dehydrogenase, which converts acetaldehyde to acetate. This reaction is one of the major routes for the metabolism of alcohol in humans. 7-Methoxy-1-naphthaldehyde can be used as a substrate in immunochemical assays, and its synthetic scheme has been published. 7MNA was also found to have cytotoxic effects on human liver cells in vitro.</p>Formula:C12H10O2Purity:Min. 95%Molecular weight:186.21 g/mol




