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 | |
| Name | 4-Methyl-1-naphthoic acid |
|---|---|
| Synonym | More Synonyms |
| Density | 1.2±0.1 g/cm3 |
|---|---|
| Boiling Point | 387.4±11.0 °C at 760 mmHg |
| Melting Point | 179-181ºC(lit.) |
| Molecular Formula | C12H10O2 |
| Molecular Weight | 186.207 |
| Flash Point | 174.0±13.9 °C |
| Exact Mass | 186.068085 |
| PSA | 37.30000 |
| LogP | 3.59 |
| Vapour Pressure | 0.0±0.9 mmHg at 25°C |
| Index of Refraction | 1.654 |
| InChIKey | SIVYRLBDAPKADZ-UHFFFAOYSA-N |
| SMILES | Cc1ccc(C(=O)O)c2ccccc12 |
| Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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| Hazard Codes | Xn |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2916399090 |
| HS Code | 2916399090 |
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| Summary | 2916399090 other aromatic monocarboxylic acids, their anhydrides, halides, peroxides, peroxyacids and their derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:30.0% |
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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 vi... |
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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) re... |
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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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| 1-Naphthalenecarboxylic acid, 4-methyl- |
| 4-Methyl-1-naphthoic acid |
| 4-Methyl-1-naphthalenecarboxylic Acid |
| MFCD00671557 |
| 4-Methyl-naphthalene-1-carboxylic acid |
| 4-methylnaphthalene-1-carboxylic acid |