CAS 2243-80-3
:3-nitrobenzophenone
Description:
3-Nitrobenzophenone is an organic compound characterized by its structure, which consists of a benzophenone core with a nitro group positioned at the meta position relative to the carbonyl group. This compound typically appears as a yellow crystalline solid and is known for its role as a photoinitiator in polymer chemistry and as an intermediate in organic synthesis. It has a relatively high melting point and is soluble in organic solvents such as ethanol and acetone, but has limited solubility in water. The presence of the nitro group contributes to its electronic properties, making it a useful compound in various chemical reactions, including electrophilic aromatic substitution. Additionally, 3-nitrobenzophenone exhibits UV-absorbing properties, which can be advantageous in applications involving UV protection. Safety considerations should be taken into account, as it may pose health risks if inhaled or ingested, and appropriate handling procedures should be followed in laboratory settings.
Formula:C13H9NO3
InChI:InChI=1/C13H9NO3/c15-13(10-5-2-1-3-6-10)11-7-4-8-12(9-11)14(16)17/h1-9H
InChI key:InChIKey=MFYLRNKOXORIPK-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(N(=O)=O)=CC=C1)C2=CC=CC=C2
Synonyms:- (3-Nitrophenyl)(Phenyl)Methanone
- (3-Nitrophenyl)phenylmethanone
- Benzophenone, 3-nitro-
- Methanone, (3-nitrophenyl)phenyl-
- NSC 37083
- m-Nitrobenzophenone
- 3-Nitrobenzophenone
- 3-Nitrobenzophenone 98%
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Found 4 products.
(3-Nitrophenyl)(phenyl)methanone
CAS:Formula:C13H9NO3Purity:98%Color and Shape:SolidMolecular weight:227.21553-Nitrobenzophenone
CAS:3-NitrobenzophenonePurity:98%Color and Shape:Tan PowderMolecular weight:227.22g/mol3-Nitrobenzophenone
CAS:<p>3-Nitrobenzophenone is a nitro compound that has been shown to undergo UV irradiation, which causes its conversion to a carbanion. This reaction proceeds with the elimination of a proton and the formation of a carbonyl group. The carbonyl group then reacts with another molecule of 3-nitrobenzophenone in an entropic transfer reaction to form the two products. Analysis of this product has shown it to be chiral, with an R configuration at the hydroxyl group and an S configuration at the carbonyl group. It also has a copper salt as well as a hydroxyl and carbonyl groups.<br>3-Nitrobenzophenone can be synthesized by reacting malonate with nitric acid in the presence of copper(II) sulfate. This reaction produces 3-nitrobenzoic acid, which is oxidized using hydrogen peroxide to yield 3-nitrobenzophenone</p>Formula:C13H9NO3Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:227.22 g/mol
