2'-Aminobenzophenone-2-carboxylic Acid TCI A1994

Chemical Identity

CAS No.: 1147-43-9
PubChem: CID 70847·SID 87559107
Formula: C14H11NO3
Molecular weight: 241.24 g/mol
Purity: >98.0%(HPLC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-(2-aminobenzoyl)benzoic acid
SMILES: C1=CC=C(C(=C1)C(=O)C2=CC=CC=C2N)C(=O)O
InChIKey: KORKIRUGUNPQML-UHFFFAOYSA-N

Rp 822.150,00

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2'-Aminobenzophenone-2-carboxylic Acid is a chemical compound widely used in laboratory experiments across chemical and biochemical research. This compound plays a crucial role in organic synthesis and peptide chemistry due to its unique molecular structure. It is commonly employed as a building block for the creation of bioactive molecules, contributing to advancements in drug discovery and molecular biology. Its versatility makes it an essential tool for researchers working on complex chemical reactions and molecular interactions.

The compound's chemical properties, including the presence of both amino and carboxyl functional groups, make it highly reactive in various chemical processes. These functional groups enable it to participate in reactions such as esterification, amidation, and substitution, which are fundamental in synthetic chemistry. Its ability to form stable intermediates under controlled conditions enhances its utility in laboratory settings. The compound's reactivity also allows it to interact with a wide range of molecules, making it ideal for studies involving molecular recognition and binding.

In Indonesian laboratories, 2'-Aminobenzophenone-2-carboxylic Acid is frequently used in research related to chemistry, pharmacy, and biotechnology. It supports investigations into the development of new pharmaceutical compounds and the understanding of molecular interactions. Its application spans across academic and industrial research, contributing to the advancement of scientific knowledge in various fields.

Related TCI products

Organic synthesis where the compound's functional groups enable the creation of complex molecules through esterification and amidation reactions.
Peptide chemistry research due to its ability to participate in amide bond formation, essential for synthesizing bioactive peptides.
Bioactive molecule development as a building block for compounds with specific biological activities in pharmaceutical research.
Molecular interaction studies because of its capacity to bind with various molecules, aiding in understanding molecular recognition processes.
Drug discovery initiatives where the compound's reactivity supports the synthesis of potential therapeutic agents.

Brand	TCI
CAS number	1147-43-9
Molecular formula	—
Purity	—
Category	Chemistry > Chemical Biology > Peptide Chemistry
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

This compound should be stored in a cool, dry place, away from direct light and sources of heat. It is recommended to use airtight containers to prevent moisture absorption, which can affect its chemical stability. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to extreme temperatures and ensure proper ventilation in the laboratory. The compound is best stored in a controlled environment to maintain its integrity and effectiveness for research applications. Always follow standard laboratory safety protocols when handling reactive chemicals.

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