13722-96-8

Basic information

• Product Name: 2,4-dihydroxy-5-nitrobenzoic acid
• Synonyms: 2,4-dihydroxy-5-nitrobenzoic acid
• CAS NO: 13722-96-8
• Molecular Formula: C₇H₅NO₆
• Molecular Weight: 199.1177
• Mol File: 13722-96-8.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,4-dihydroxy-5-nitrobenzoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4-dihydroxy-5-nitrobenzoic acid(13722-96-8)
• EPA Substance Registry System: 2,4-dihydroxy-5-nitrobenzoic acid(13722-96-8)

Safety Data

• Hazardous Substances Data: 13722-96-8(Hazardous Substances Data)

Usage

General Description

2,4-dihydroxy-5-nitrobenzoic acid is a compound with the chemical formula C7H5NO6. It is a derivative of benzoic acid and consists of a benzene ring with two hydroxyl groups and one nitro group attached. The compound is a yellow crystalline solid at room temperature and is commonly used as a reagent in organic synthesis and as a precursor to other chemicals. It is also known for its antibacterial and antifungal properties and has potential applications in the pharmaceutical and agricultural industries. Additionally, 2,4-dihydroxy-5-nitrobenzoic acid is a key intermediate in the synthesis of pigments and dyes, and it is also used as a pH indicator in chemical laboratory experiments.

Upstream product

• 89-86-1 4-hydroxysalicylic acid 
• 13722-95-7 4-hydroxy-5-nitrosalicylate 
• 7697-37-2 nitric acid 
• 271261-71-3 2,4-dihydroxy-5-nitro-benzoic acid methyl ester 
• 108-46-3 recorcinol 

Downstream Products

• 81574-75-6 2,4-dimethoxy-5-nitro-benzoic acid methyl ester 
• 59036-73-6 2,4-diethoxy-5-nitro-benzoic acid ethyl ester 
• 271261-71-3 2,4-dihydroxy-5-nitro-benzoic acid methyl ester 
• 3163-07-3 4-nitroresorcinol 
• 69938-56-3 5-amino-2,4-dihydroxybenzoic acid 
• 855875-92-2 3-chloro-2,4-dihydroxy-5-nitro-benzoic acid 
• 22604-84-8 2,4-dihydroxy-3,5-dinitro-benzoic acid 
• 720672-26-4 3-bromo-2,4-dihydroxy-5-nitro-benzoic acid 
• 15719-64-9 methylammonium carbonate 
• 874210-23-8 2,4-bis[3-(ethoxycarbonyl)propoxy]-5-nitrobenzoic acid 
• 271261-72-4 5-nitro-2,4-bis(octyloxy)benzoic acid methyl ester 
• 874210-16-9 2,4-bis[3-(tert-butoxycarbonyl)propoxy]-5-nitrobenzoic acid methyl ester 
• 874210-15-8 2,4-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}-5-nitrobenzoic acid methyl ester 
• 874210-20-5 2,4-bis[3-(tert-butoxycarbonyl)propoxy]-5-nitrobenzoic acid 

Relevant articles and documents

Multiturn Hollow Helices: Synthesis and Folding of Long Aromatic Oligoamides

Aromatic oligoamides adopting helical conformations are synthesized by coupling carboxyl-terminated basic units having two, four, and eight residues to amine-terminated oligomer precursors. Coupling yields show no noticeable reduction with the size of the

Preparation method for 5-amino-2,4-dihydroxybenzoic acid

The invention provides a preparation method for 5-amino-2,4-dihydroxybenzoic acid. The method comprises the steps that the raw material 2,4-dihydroxybenzoic acid is provided; the 2,4-dihydroxybenzoicacid is subjected to a nitration reaction to generate 5-

Diversity-oriented synthesis for novel, selective and drug-like inhibitors for a phosphatase from Mycobacterium tuberculosis

Mycobacterium protein tyrosine phosphatase B (mPTPB) is a potential drug target of tuberculosis (TB). Using small molecule inhibitors of mPTPB could be a treatment to overcome emerging TB drug resistance. Using a Diversity-Oriented Synthesis (DOS) strateg