CAS 33738-48-6
:4-methylnaphthalene-1-carbaldehyde
Description:
4-Methylnaphthalene-1-carbaldehyde, with the CAS number 33738-48-6, is an organic compound characterized by its naphthalene structure, which consists of two fused aromatic rings. This compound features a methyl group and an aldehyde functional group, contributing to its reactivity and potential applications in organic synthesis. It typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the aldehyde group makes it a useful intermediate in the synthesis of various chemical compounds, including pharmaceuticals and agrochemicals. Additionally, 4-methylnaphthalene-1-carbaldehyde may exhibit distinct aromatic properties, influencing its behavior in chemical reactions and interactions with other substances. Its solubility is generally higher in organic solvents than in water, which is common for many aromatic compounds. Safety considerations should be taken into account when handling this substance, as it may pose health risks if inhaled or ingested, and appropriate protective measures should be employed in laboratory settings.
Formula:C12H10O
InChI:InChI=1/C12H10O/c1-9-6-7-10(8-13)12-5-3-2-4-11(9)12/h2-8H,1H3
SMILES:Cc1ccc(C=O)c2ccccc12
Synonyms:- 1-Naphthalenecarboxaldehyde, 4-methyl-
- 4-Methyl-1-naphthaldehyde
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Found 5 products.
4-Methyl-1-naphthaldehyde
CAS:Formula:C12H10OPurity:98%Color and Shape:SolidMolecular weight:170.20724-Methyl-1-naphthaldehyde
CAS:Controlled Product<p>Applications 4-Methyl-1-naphthaldehyde is a reagent used in the preparation and immunosuppressive activity of lactones via ring-closing metathesis of alkadienes.<br>References Lee, S., et al.: Bioorg. Med. Chem. Lett., 21, 5726 (2011); Hagen, S., et al.: J. Med. Chem., 40, 3707 (1997); Buck, S., et al.: J. Am. Chem. Soc., 125, 15694 (125)<br></p>Formula:C12H10OColor and Shape:NeatMolecular weight:170.2074-Methyl-1-naphthaldehyde
CAS:4-Methyl-1-naphthaldehyde is a chemical compound that is found in cigarette smoke and also has been detected in the microenvironment of pancreatic cancer cells. This substance is a precursor to the carcinogenic naphthalene, which reacts with ammonium nitrate to form nitrosoamines. 4-Methyl-1-naphthaldehyde inhibits tumor cell growth by binding to topoisomerase and inhibiting DNA synthesis. The molecule's ability to react with amines may be responsible for its inhibitory properties on tumor cells. The molecular orbital descriptor for this substance is 1,3,5,6,8,11,13,15,18–octahydroindolo[2′,3′:2″-c]benzofuro[3′,4′:5″-c]pyrrolo[1′,- 2″:1″']hexol.Formula:C12H10OPurity:Min. 95%Molecular weight:170.21 g/mol





