Weight | 151.121 g/mol |
---|---|
Formula | C7H5NO3 |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 2 |
2-NITROBENZALDEHYDE (31620-90-3, 552-89-6)
o-nitrobenzaldehyde · ortho-nitrobenzaldehyde
Score:
#79 in Physical chemistry
,
#2021 in Physics
,
#6307 in Chemistry
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- Photochemistry of o-nitrobenzaldehyde and related studies (The Journal of Physical Chemistry, 1980)
- Ultra Sensitive, Specific Method for Cyanide Using p-Nitrobenzaldehyde and o-Dinitrobenzene. (Analytical Chemistry, 1966)
- 2-Nitrobenzaldehyde as a chemical actinometer for solution and ice photochemistry (Journal of Photochemistry and Photobiology A-chemistry, 2010)
- The Photochemistry of oNitrobenzaldehyde as Seen by Femtosecond Vibrational Spectroscopy (Angewandte Chemie, 2005)
- Palladium complex-catalyzed intermolecular reductive N-heterocyclization: novel synthesis of quinazoline derivatives from 2-nitrobenzaldehyde or 2-nitrophenyl ketones with formamide (Journal of Organometallic Chemistry, 1995)
- Studies on Some Schiff Base Complexes of CoII, NiII and CuII Derived from Salicylaldehyde and O-Nitrobenzaldehyde (Spectroscopy Letters, 1998)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - o-nitrobenzaldehyde
- ortho-nitrobenzaldehyde
-
SMILESC1=CC=C(C(=C1)C=O)[N+](=O)[O-]
-
InChIKeyCMWKITSNTDAEDT-UHFFFAOYSA-N
- Pubchem - 2-NITROBENZALDEHYDE
- Wikipedia - 2-Nitrobenzaldehyde
2-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group ortho to formyl. 2-Nitrobenzaldehyde once was produced as an intermediate in the synthesis of the popular dye Indigo.
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