CAS 19176-60-4

4-nitrophenyl anthranilate

Description:

4-Nitrophenyl anthranilate is an organic compound characterized by its structure, which includes an anthranilic acid moiety and a nitrophenyl group. This compound typically appears as a yellow crystalline solid and is known for its potential applications in various fields, including pharmaceuticals and dye synthesis. The presence of the nitro group contributes to its reactivity and can influence its solubility and stability in different solvents. It is generally soluble in organic solvents but may have limited solubility in water. The compound exhibits properties typical of both aromatic amines and nitro compounds, which can affect its behavior in chemical reactions, such as electrophilic substitution or nucleophilic attack. Additionally, 4-nitrophenyl anthranilate may show biological activity, making it of interest in medicinal chemistry. Safety considerations should be taken into account due to the potential toxicity associated with nitro compounds. Overall, its unique structural features and reactivity make it a compound of interest in various chemical research areas.

Formula: C₁₃H₁₀N₂O₄

InChI: InChI=1/C13H10N2O4/c14-11-8-10(15(17)18)6-7-12(11)19-13(16)9-4-2-1-3-5-9/h1-8H,14H2

SMILES: c1ccc(cc1)C(=O)Oc1ccc(cc1N)N(=O)=O

Synonyms:

• Anthralinic acid 4-Nitrophenyl ester
• 1,3-Bis(Bromomethyl)-5-Methylbenzene

4-Nitrophenyl 2-Aminobenzoate

CAS: 19176-60-4

Formula: C₁₃H₁₀N₂O₄

Purity: >98.0%(N)

Color and Shape: Light yellow to Yellow to Orange powder to crystal

Molecular weight: 258.23

Ref: 3B-A0842

Benzoic acid, 2-amino-, 4-nitrophenyl ester

CAS: 19176-60-4

Formula: C₁₃H₁₀N₂O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 258.2295

Ref: IN-DA002FGM

4-Nitrophenyl anthranilate

CAS: 19176-60-4

Formula: C₁₃H₁₀N₂O₄

Purity: 98%

Color and Shape: Solid

Molecular weight: 258.233

Ref: 10-F018908

4-Nitrophenyl Anthranilate

Controlled Product

CAS: 19176-60-4

4-Nitrophenyl anthranilate is a potent inhibitor of serine protease. It is synthesized by reacting an anthranilate with an hydroxyl group in the presence of ultraviolet light, and can be used as a fluorescent probe. 4-Nitrophenyl anthranilate binds to the active site of serine protease, and prevents the hydrolysis of proteins by blocking the cleavage of peptide bonds at the carboxylic acid termini. This compound has been shown to inhibit human serum albumin and cell nuclei in vitro. The reaction mechanism for this compound is unknown, but it is believed that it may involve a photo-induced electron transfer mechanism.

Formula: C₁₃H₁₀N₂O₄

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 258.23 g/mol

Ref: 3D-FN61994