CAS 782-45-6

4-Amino-N-phenylbenzamide

Description:

4-Amino-N-phenylbenzamide, also known as 4-Aminobenzamide, is an organic compound characterized by its amine and amide functional groups. It features a phenyl group attached to a benzamide structure, which contributes to its chemical reactivity and properties. This compound typically appears as a white to light yellow crystalline solid and is soluble in polar solvents such as water and alcohols. The presence of the amino group allows for potential hydrogen bonding, influencing its solubility and interaction with other molecules. 4-Amino-N-phenylbenzamide is often utilized in various chemical syntheses and can serve as a precursor in the production of pharmaceuticals and agrochemicals. Its reactivity can be attributed to the electron-donating nature of the amino group, which can enhance nucleophilicity. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Safety data should be consulted, as with any chemical, to understand its handling and potential hazards.

Formula: C₁₃H₁₂N₂O

InChI: InChI=1S/C13H12N2O/c14-11-8-6-10(7-9-11)13(16)15-12-4-2-1-3-5-12/h1-9H,14H2,(H,15,16)

InChI key: InChIKey=QHWDUJPWCGEBTH-UHFFFAOYSA-N

SMILES: C(NC1=CC=CC=C1)(=O)C2=CC=C(N)C=C2

Synonyms:

• 1-Aminobenzene-4-carboxylic acid phenylamide
• 4-amino-N-phenylbenzamide
• Aminobenzaldehydepolymer
• Benzamide, 4-amino-N-phenyl-
• Benzanilide, 4-amino-
• Ethyl 3-(Trimethylsilyl)Propanoate
• Fast Red Base DB-90
• N-(4-Aminophenyl)benzamide
• N-Phenyl-4-aminobenzamide
• 4'-aminobenzanilide
• 4-Aminobenzanilide

4-Amino-N-phenylbenzamide

CAS: 782-45-6

Formula: C₁₃H₁₂N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 212.2472

Ref: IN-DA003KRT

4-Amino-N-phenylbenzamide

CAS: 782-45-6

4-Amino-N-phenylbenzamide

Purity: 98%

Molecular weight: 212.25g/mol

Ref: 54-OR96489

4-Aminobenzanilide

CAS: 782-45-6

4-Aminobenzanilide is an antimicrobial agent that is synthesized from 2-aminobenzamide and 4-aminophenol. It has been shown to be effective against a number of bacteria, including Staphylococcus aureus and Streptococcus pyogenes. 4-Aminobenzanilide has also been shown to inhibit the growth of Mycoplasma pneumoniae in mammalian cells, which may be due to its ability to block DNA replication and transcription. This compound can also disrupt the synthesis of amides by inhibiting the enzyme aminopeptidase N. The low energy required for this reaction makes it possible for this compound to work as an antimicrobial agent with minimal toxicity.

Formula: C₁₃H₁₂N₂O

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 212.25 g/mol

Ref: 3D-FA71280

4-amino-N-phenylbenzamide

CAS: 782-45-6

Formula: C₁₃H₁₂N₂O

Purity: 97%

Color and Shape: Solid

Molecular weight: 212.252

Ref: 10-F355603