1-NITRO-2-NAPHTHALDEHYDE

Names

[ Name ]:
1-NITRO-2-NAPHTHALDEHYDE

[Synonym ]:
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

Chemical & Physical Properties

[ Density]:
1.368g/cm3

[ 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

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
Xi

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2913000090

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Customs

[ HS Code ]: 2913000090

[ 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%

Articles

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,...

Materials and systems for two photon 3-D ROM devices. Dvornikov AS, et al.

IEEE Trans. Compon. Packag. Tech. 20(2) , 203-212, (1997)