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TCI

CAS 1144-74-7

4-Nitrobenzophenone TCI N0365

4-Nitrobenzophenone TCI N0365

Chemical Identity

CAS No.
1144-74-7
PubChem
CID 70839·SID 87573716
Formula
C13H9NO3
Molecular weight
227.21 g/mol
Purity
>99.0%(GC)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(4-nitrophenyl)-phenylmethanone
SMILES
C1=CC=C(C=C1)C(=O)C2=CC=C(C=C2)[N+](=O)[O-]
InChIKey
ZYMCBJWUWHHVRX-UHFFFAOYSA-N
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4-Nitrobenzophenone is a versatile organic compound widely used in laboratory settings for its reactivity and structural versatility. It belongs to the class of non-heterocyclic building blocks and is commonly employed in organic synthesis for the preparation of aromatic and heterocyclic compounds. Its molecular structure, featuring a benzophenone core with a nitro group, makes it a valuable intermediate in various chemical reactions. This compound is particularly useful in synthetic pathways where controlled reactivity and functional group compatibility are essential.

The compound's chemical properties, including its stability and reactivity, make it a preferred choice in both academic and industrial research. It exhibits unique reactivity in reactions such as Diels-Alder, Michael, and photoreduction, making it suitable for complex synthetic strategies. Additionally, its aromatic structure allows for UV light absorption, which is beneficial in photochemical processes. These characteristics contribute to its widespread use in the development of new materials and pharmaceutical compounds.

In Indonesian laboratories, 4-Nitrobenzophenone is a key component in chemical research, particularly in the development of pharmaceuticals, industrial chemicals, and polymer materials. It is frequently used in educational institutions and research facilities for teaching and experimental purposes. Its role in both basic and applied research underscores its importance in the chemical sciences.

  • Organic synthesis for the preparation of aromatic and heterocyclic compounds due to its reactivity and structural versatility.
  • Photoreduction and photochemical reactions because of its ability to absorb UV light and participate in light-induced transformations.
  • Development of pharmaceutical compounds as a building block in the synthesis of drug molecules and active pharmaceutical ingredients.
  • Research in polymer science for the creation of advanced materials with specific optical and chemical properties.
  • Educational use in teaching organic chemistry and reaction mechanisms to students and researchers.

Brand TCI
CAS number 1144-74-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

4-Nitrobenzophenone should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its potential reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with strong acids or bases to prevent unwanted chemical reactions. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling this compound. It is important to ensure that storage conditions are suitable for long-term preservation and safe use in laboratory settings.

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