3558-18-7

Usage

Uses

Used in Pharmaceutical Synthesis:
2-(Acetylamino)-5-nitrobenzoic acid is used as an intermediate in the production of various types of drugs, contributing to the development of new medications.
Used in Organic Dye Production:
2-(ACETYLAMINO)-5-NITROBENZOIC ACID is used as a component in the synthesis of organic dyes, providing color to various products.
Used in Anti-Microbial Research:
2-(Acetylamino)-5-nitrobenzoic acid is studied for its anti-microbial properties, indicating its potential use in the development of antimicrobial agents.
Used in Novel Pharmaceutical Development:
The presence of the nitro group in the molecule makes 2-(Acetylamino)-5-nitrobenzoic acid a potential candidate for further research in the development of novel pharmaceuticals, exploring its potential in treating various conditions.

InChI:InChI=1/C9H8N2O5/c1-5(12)10-8-3-2-6(11(15)16)4-7(8)9(13)14/h2-4H,1H3,(H,10,12)(H,13,14)

Upstream product

• 108-24-7 acetic anhydride 
• 616-79-5 2-amino-5-nitro-benzoic acid 
• 10073-89-9 2-methyl-6-nitro-4H-benzo[d][1,3]oxazin-4-one 
• 7732-18-5 water 
• 120-66-1 N-(2-methylphenyl)acetamide 
• 99-52-5 2-methyl-4-nitro-benzenamine 
• 13138-53-9 4-nitrophthalic amide 
• 118-92-3 anthranilic acid 
• 91538-60-2 N-(2-formyl-4-nitrophenyl)acetamide 
• 7697-37-2 nitric acid 
• 89-52-1 o-acetylamino-benzoic acid 
• 2719-15-5 2-methyl-4-nitroacetanilide 

Downstream Products

• 54669-98-6 2-Acetylamino-5-amino-benzoic acid 
• 616-79-5 2-amino-5-nitro-benzoic acid 
• 123524-73-2 2-mercapto-6-nitro-3-(4-methyl-phenyl)quinazolin-4(3H)-one 
• 100-01-6 4-nitro-aniline 
• 123524-74-3 2-mercapto-3-(2',4'-dichlorostilbenyl)-6-nitro-4-oxoquinazoline 
• 1194506-70-1 C₁₇H₁₁ClN₄O₂ 

Relevant academic research and scientific papers

NITROGEN-CONTAINING HETEROCYCLIC COMPOUNDS AND BENAMIDE COMPOUNDS AND DRUGS CONTAINING THE SAME

Disclosed are compounds represented by formula (I) which have triglyceride biosynthesis inhibitory activity in the liver and inhibitory activity against the secretion of apolipoprotein B-containing lipoprotein from the liver and particularly have excellent inhibitory activity against the secretion of apolipoprotein B-containing lipoprotein, are free from side effect of accumulation of lipids in the liver, and are useful for the treatment and prevention of hyperlipidemia and arteriosclerotic diseases. In formula (I), R1 and R2 represent alkyl, alkoxy, cycloalkyl, phenyl, alkenyl, alkynyl, or a five- or six-membered saturated or unsaturated heterocyclic ring, or R1 and R2, together with a nitrogen atom to which R1 and R2 are attached, may form a ring; R3 and R4 represent a hydrogen atom, alkyl, a halogen atom, hydroxyl, nitrile, alkoxycarbonyl, alkoxy, or carboxyl; or R2 and R3 may be attached to each other to form -(CH2)m-, -N=CH-, -CH=N-, or -(C1-6 alkyl)C=N-; A, D, E, and G each represent a carbon atom, or any one of A, D, E, and G represents a nitrogen atom with the other three each representing a carbon atom; Q represents a nitrogen atom or a carbon atom; Y represents a group represented by formula (II) wherein X represents a hydrogen atom, group -C(=O)N(R5)R6 or group -C(=O)OR7, R8 is absent or represents a bond, an oxygen atom, a sulfur atom, -SO2-, -SO-, -CH2-CH2-, or - CH=CH-, and R9 and R10 represent a hydrogen atom, alkyl, alkoxy, a halogen atom, or hydroxyl; and Z represents - (CH2)n-, -O-(CH2)i-, or -C(=O)NH-(CH2)i-.

Synthesis and application of novel heterocyclic dyes based on 11-Amino-3-Bromo-13H-acenaphtho[1,2-e]pyridazino[3,2-b]-quinazoline-13-one

Synthesized a new fused heterocyclic compound, 11-Amino-3-Bromo-13H-acenaphtho[1,2-e]pyridazino[3,2-b]-quinazoline-13-one and is used to synthesize a novel series of heterocyclic mono azo dyes by coupling with various naphthols. All the dyes were characterized by their percentage yield, melting point, UV-visible spectroscopy, elemental analysis, infrared spectroscopy and dyeing performance on nylon 66 and polyester fibres. The percentage dye bath exhaustion on different fibres has been found to be reasonably good and acceptable. The dyed fibres showed fair to fairly good fastness to light and very good to excellent fastness to washing, rubbing, perspiration and sublimation.

Diaminopuridine-containing thiourea inhibitors of herpes viruses

Compounds of the formula STR1 are useful in the treatment of diseases associated with herpes viruses including human cytomegalovirus, herpes simplex viruses, Epstein-Barr virus, varicella-zoster virus, human herpesviruses-6 and -7, and Kaposi herpesvirus.