5-Chloro-2-(methylamino)benzophenone TCI C2281

Chemical Identity

CAS No.: 1022-13-5
PubChem: CID 13925·SID 87561015
Formula: C14H12ClNO
Molecular weight: 245.71 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: [5-chloro-2-(methylamino)phenyl]-phenylmethanone
SMILES: CNC1=C(C=C(C=C1)Cl)C(=O)C2=CC=CC=C2
InChIKey: WPNMLCMTDCANOZ-UHFFFAOYSA-N
MDL: MDL00008284

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5-Chloro-2-(methylamino)benzophenone is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It plays a crucial role in laboratory settings where the creation of aromatic compounds with intricate structures is required. This compound is commonly employed in organic reactions, particularly in the formation of aromatic derivatives with multiple functional groups. Its versatility and reactivity make it an essential component in various chemical experiments and research projects.

The compound is known for its stable molecular structure and its ability to readily react with a variety of reagents. This reactivity, combined with its capacity to form bonds with amino and chloro groups, makes it a preferred choice for chemists working on synthetic pathways. Its chemical properties allow for the development of new compounds with complex structures, which are vital in both academic and industrial research. The compound's functional group compatibility enhances its utility in a wide range of chemical transformations.

In Indonesian laboratories, 5-Chloro-2-(methylamino)benzophenone is a key reagent used in both fundamental and applied chemical research. It is frequently utilized in the synthesis of aromatic compounds and in drug development projects. Research institutions and universities across Indonesia rely on this compound for experiments that require precise chemical reactions and the formation of complex molecular structures. Its consistent performance and reliability make it a staple in many chemical laboratories.

Related TCI products

Synthesis of complex aromatic compounds for pharmaceutical development due to its reactivity with amino and chloro groups.
Organic reaction pathways requiring substitution of chloro groups in heterocyclic compound formation.
Development of new chemical structures through functional group modifications in synthetic chemistry.
Research in medicinal chemistry for the creation of novel drug molecules with specific structural features.
Experimental studies in chemical synthesis focusing on the formation of stable aromatic derivatives.

Brand	TCI
CAS number	1022-13-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	As per supplier specifications
Physical form	Solid (as per standard product description)
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 moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its stability. Proper ventilation should be maintained in the laboratory to ensure safe handling. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to keep the compound away from incompatible substances to prevent unwanted chemical reactions. Always follow standard laboratory safety protocols when working with this material.

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