1,4-Dimethoxynaphthalene structure
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Common Name | 1,4-Dimethoxynaphthalene | ||
|---|---|---|---|---|
| CAS Number | 10075-62-4 | Molecular Weight | 188.22200 | |
| Density | 1.097 g/cm3 | Boiling Point | 317.6ºC at 760 mmHg | |
| Molecular Formula | C12H12O2 | Melting Point | 85 °C | |
| MSDS | Chinese USA | Flash Point | 134.3ºC | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Synthetic Studies on the Kinamycin Family of Antibiotics: Synthesis of 2-(Diazobenzyl)-p-naphthoquinone, 1,7-Dideoxy-3-demethylprekinamycin, and 1-Deoxy-3-demethylprekinamycin.
J. Org. Chem. 62(13) , 4364-4369, (1997) 2-(Diazobenzyl)-p-naphthoquinone was synthesized from 2-benzyl-1,4-dimethoxynaphthalene by cerric ammonium nitrate oxidation to 2-benzyl-p-naphthoquinone followed by diazo transfer with tosyl azide. 1,7-Dideoxy-3-demethylprekinamycin was prepared from 1,4-dim... |
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Synthesis of new arylalkoxy amido derivatives as melatoninergic ligands.
Bioorg. Med. Chem. 11 , 789-800, (2003) Amido derivatives 10-18 of the corresponding oxyamines were synthesised as melatoninergic ligands by the reaction of hydroxyphtalimide with the halogeno derivatives or the corresponding alcohols using Mitsunobu reaction conditions. The affinity of the compoun... |
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Two new naphthalene and anthraquinone derivatives from Asphodelus tenuifolius.
Pharmazie 57 , 286-287, (2002) Chromatographic separation of an ethanolic extract of rhizomes of Asphodelus tenuifolius Cav. (Asphodelaceae) yielded in addition to beta-sitosterol, stigmasterol and two anthraquinone derivatives, 1,8-dimethoxynaphthalene as well as two new naphthalene deriv... |
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Novel haloacetoxylation of 1, 4-dimethoxynaphthalenes using hypervalent iodine chemistry. Evans PA and Brandt TA.
Tetrahedron Lett. 27(36) , 6443-46, (1996)
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