1-NITRO-2-NAPHTHALDEHYDE structure
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Common Name | 1-NITRO-2-NAPHTHALDEHYDE | ||
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CAS Number | 101327-84-8 | Molecular Weight | 201.17800 | |
Density | 1.368g/cm3 | Boiling Point | 384.6ºC at 760 mmHg | |
Molecular Formula | C11H7NO3 | Melting Point | 109-110ºC(lit.) | |
MSDS | Chinese USA | Flash Point | 197.5ºC |
Name | 1-nitronaphthalene-2-carbaldehyde |
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Synonym | More Synonyms |
Density | 1.368g/cm3 |
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Boiling Point | 384.6ºC at 760 mmHg |
Melting Point | 109-110ºC(lit.) |
Molecular Formula | C11H7NO3 |
Molecular Weight | 201.17800 |
Flash Point | 197.5ºC |
Exact Mass | 201.04300 |
PSA | 62.89000 |
LogP | 3.08370 |
Vapour Pressure | 4.05E-06mmHg at 25°C |
Index of Refraction | 1.708 |
Personal Protective Equipment | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
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Hazard Codes | Xi |
RIDADR | NONH for all modes of transport |
HS Code | 2913000090 |
HS Code | 2913000090 |
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Summary | HS: 2913000090 halogenated, sulphonated, nitrated or nitrosated derivatives of products of heading 2912 Educational tariff:17.0% Tax rebate rate:9.0% Regulatory conditions:none Most favored nation tariff:5.5% General tariff:30.0% |
The Baylis-Hillman acetates as a valuable source for one-pot multistep synthesis: a facile synthesis of functionalized tri-/tetracyclic frameworks containing azocine moiety.
Org. Lett. 9(13) , 2453-6, (2007) The Baylis-Hillman acetates have been conveniently transformed into tri-/tetracyclic heterocyclic frameworks containing an important azocine moiety via one-pot multistep protocol involving alkylation,... |
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Materials and systems for two photon 3-D ROM devices. Dvornikov AS, et al.
IEEE Trans. Compon. Packag. Tech. 20(2) , 203-212, (1997)
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1-nitro-2-naphthalenecarboxaldehyde |
1-nitro-[2]naphthaldehyde |
1-nitronaphthalene-2-carboxaldehyde |
MFCD03427164 |
2-Naphthalenecarboxaldehyde,1-nitro |
1-nitro-2-naphthylaldehyde |
1-nitro-naphthalene-2-carbaldehyde |