4-Methyl-1-naphthoic acid
4-Methyl-1-naphthoic acid structure
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Common Name | 4-Methyl-1-naphthoic acid | ||
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| CAS Number | 4488-40-8 | Molecular Weight | 186.207 | |
| Density | 1.2±0.1 g/cm3 | Boiling Point | 387.4±11.0 °C at 760 mmHg | |
| Molecular Formula | C12H10O2 | Melting Point | 179-181ºC(lit.) | |
| MSDS | Chinese USA | Flash Point | 174.0±13.9 °C | |
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Iron-catalyzed cross-dehydrogenative coupling esterification of unactive C(sp3)-H bonds with carboxylic acids for the synthesis of α-acyloxy ethers.
J. Org. Chem. 79(9) , 3847-55, (2014) An iron-catalyzed oxidative esterification reaction between unactivated C(sp(3))-H bonds from symmetric and asymmetric ethers and carboxylic acids using di-tert-butyl peroxide (DTBP) as the oxidant via a cross dehydrogenative coupling (CDC) reaction was estab... |
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Structure-activity relationships for 1-alkyl-3-(1-naphthoyl)indoles at the cannabinoid CB(1) and CB(2) receptors: steric and electronic effects of naphthoyl substituents. New highly selective CB(2) receptor agonists.
Bioorg. Med. Chem. 13(1) , 89-112, (2005) In an effort to improve indole-based CB(2) cannabinoid receptor ligands and also to develop SAR for both the CB(1) and CB(2) receptors, 47 indole derivatives were prepared and their CB(1) and CB(2) receptor affinities were determined. The indole derivatives i... |
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Preparation of a series of substituted fluoromethylnaphthalenes. Dixon EA, et al.
Can. J. Chem. 59(17) , 2629-2641, (1981)
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