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 | |
| Name | 1,4-dimethoxynaphthalene |
|---|---|
| Synonym | More Synonyms |
| Density | 1.097 g/cm3 |
|---|---|
| Boiling Point | 317.6ºC at 760 mmHg |
| Melting Point | 85 °C |
| Molecular Formula | C12H12O2 |
| Molecular Weight | 188.22200 |
| Flash Point | 134.3ºC |
| Exact Mass | 188.08400 |
| PSA | 18.46000 |
| LogP | 2.85700 |
| Vapour Pressure | 0.000708mmHg at 25°C |
| Index of Refraction | 1.584 |
| InChIKey | FWWRTYBQQDXLDD-UHFFFAOYSA-N |
| SMILES | COc1ccc(OC)c2ccccc12 |
| Storage condition | 2-8°C |
| Symbol |
GHS07 |
|---|---|
| Signal Word | Warning |
| Hazard Statements | H315-H319-H335 |
| Precautionary Statements | P261-P305 + P351 + P338 |
| Personal Protective Equipment | dust mask type N95 (US);Eyeshields;Gloves |
| Hazard Codes | Xi: Irritant; |
| Risk Phrases | R36/37/38 |
| Safety Phrases | S26 |
| RIDADR | NONH for all modes of transport |
| WGK Germany | 3 |
| HS Code | 2909309090 |
| HS Code | 2909309090 |
|---|---|
| Summary | 2909309090 other aromatic ethers and their halogenated, sulphonated, nitrated or nitrosated derivatives VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:5.5% General tariff:30.0% |
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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... |
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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... |
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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,... |
| EINECS 233-209-2 |
| Naphthalene,1,4-dimethoxy |
| 1,4-dimethoxy-naphthalene |
| Naphthalene,4-dimethoxy |
| 1,4-Dimethoxynaphthoquinone |
| MFCD00052378 |
| 1,4-Dimethoxy-naphthalin |