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About This Item
Linear Formula:
O2NC10H6CHO
CAS Number:
Molecular Weight:
201.18
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
form
solid
mp
109-110 °C (lit.)
functional group
aldehyde
nitro
SMILES string
[O-][N+](=O)c1c(C=O)ccc2ccccc12
InChI
1S/C11H7NO3/c13-7-9-6-5-8-3-1-2-4-10(8)11(9)12(14)15/h1-7H
InChI key
XQIMHJNMEFIADP-UHFFFAOYSA-N
Related Categories
General description
On irradiation with UV light, 1-nitro-2-naphthaldehyde gets transformed into the corresponding nitroso acid.
Application
1-Nitro-2-naphthaldehyde (NAA) may be used to prepare the precursors required for the preparation of 3-acetoxy-2-methylene-3-(1-nitronaphth-2-yl)propanoate and ethyl 3-acetoxy-2-methylene-3-(1-nitronaphth-2-yl)propanoate.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Materials and systems for two photon 3-D ROM devices.
Dvornikov AS, et al.
IEEE Transactions on Components and Packaging Technologies, 20(2), 203-212 (1997)
Deevi Basavaiah et al.
Organic letters, 9(13), 2453-2456 (2007-06-01)
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, reduction, and cyclization sequence.
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