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About This Item
Linear Formula:
CH3C10H6CHO
CAS Number:
Molecular Weight:
170.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
assay
97%
mp
32-36 °C (lit.)
SMILES string
Cc1ccc(C=O)c2ccccc12
InChI
1S/C12H10O/c1-9-6-7-10(8-13)12-5-3-2-4-11(9)12/h2-8H,1H3
InChI key
LANRGTXVAPBSIA-UHFFFAOYSA-N
General description
4-Methyl-1-naphthaldehyde is a monoaldehyde. It is obtained along with 1-methyl-2-naphthaldehyde from 1-methylnaphthalene, via formylation.
Application
4-Methyl-1-naphthaldehyde may be used in the synthesis of methyl 2-phenyl-3-( 4-methyl-1-naphthyl)propenoate and (Z/E)-2-amino-4,6-dimethyl-5-[(4-methyl-1-naphthyl)methylene]-5H-cyclopenta[b]pyridine-3,7-dicarbonitrile.
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Certificates of Analysis (COA)
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S Amin et al.
Chemical research in toxicology, 1(6), 349-355 (1988-11-01)
Previous studies have shown that 5-methylchrysene (5-MeC) is more carcinogenic on mouse skin than the other methylchrysenes and that the structural requirements favoring tumorigenicity of methylated polynuclear aromatic hydrocarbons are the presence of a bay region methyl group and free
The influence of aromatic compound protonation on the regioselectivity of Gattermann-Koch formylation.
Tanaka M, et al.
Chemical Communications (Cambridge, England), 2, 159-160 (1996)
Stéphanie Kolb et al.
European journal of medicinal chemistry, 45(3), 896-901 (2009-12-09)
We report herein the synthesis of 5-substituted [1]pyrindine derivatives and the evaluation of their antiproliferative properties on HeLa cells, a cervical carcinoma tumor cell line, and on the melanoma A2058 cell line. The most efficient compounds display cytotoxicity against tumor
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