1,4-Dimethoxynaphthalene structure
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Common Name | 1,4-Dimethoxynaphthalene | ||
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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 |
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Synonym | More Synonyms |
Density | 1.097 g/cm3 |
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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 |
Storage condition | 2-8°C |
Symbol |
GHS07 |
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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 |
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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% |
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 |