2-Amino-2'-chloro-5-nitrobenzophenone TCI A1754

Chemical Identity

CAS No.: 2011-66-7
PubChem: CID 74830·SID 87560924
Formula: C13H9ClN2O3
Molecular weight: 276.67 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2-amino-5-nitrophenyl)-(2-chlorophenyl)methanone
SMILES: C1=CC=C(C(=C1)C(=O)C2=C(C=CC(=C2)[N+](=O)[O-])N)Cl
InChIKey: GRDGBWVSVMLKBV-UHFFFAOYSA-N

Rp 1.881.600,00

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2-Amino-2'-chloro-5-nitrobenzophenone is a versatile organic compound widely used in laboratory settings for the synthesis of complex molecules. As a key building block in organic chemistry, it serves as a foundational material for creating a wide range of chemical structures. Its unique combination of functional groups makes it an essential reagent in both academic and industrial research. This compound is commonly employed in the development of pharmaceuticals, materials science, and other advanced chemical applications.

The compound's chemical structure features an amino group, a chloro group, and a nitro group, which contribute to its reactivity and functional versatility. These groups allow for a variety of chemical transformations, including nitration, substitution, and redox reactions. The presence of multiple reactive sites enhances its utility in synthetic pathways, enabling chemists to tailor the final product to specific needs. Its stability and predictable behavior under controlled conditions make it a preferred choice for laboratory use.

In Indonesian laboratories, 2-Amino-2'-chloro-5-nitrobenzophenone is frequently utilized in organic chemistry research, particularly in pharmaceutical and material science projects. Local researchers rely on its structural adaptability to develop new compounds with potential clinical or industrial applications. Its role in synthesizing complex molecules makes it an important resource for innovation in chemical research.

Related TCI products

Organic synthesis for the development of pharmaceutical compounds due to its reactive functional groups and structural versatility.
Nitration reactions where the nitro group can be selectively modified to create diverse derivatives.
Substitution reactions to introduce or replace functional groups, enabling the creation of new molecular frameworks.
Redox processes where the compound's electron-rich nature facilitates oxidation or reduction pathways.
Material science research for the synthesis of advanced polymers and functional materials with tailored properties.

Brand	TCI
CAS number	2011-66-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and maintain its chemical integrity. Due to its reactive nature, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and safety goggles should be worn. Avoid contact with incompatible substances, and ensure proper disposal according to local regulations. Regular inspection of storage conditions is advised to ensure long-term stability and safety in laboratory settings.

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