271261-71-3

Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 2,4-dihydroxy-5-nitro-, methyl ester (9CI) is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its cytotoxic properties make it a candidate for the development of anticancer drugs, targeting cancer cells and inhibiting their growth. Additionally, its antimicrobial properties can be utilized in the formulation of antimicrobial agents to combat bacterial infections.
Used in Dye and Fragrance Industry:
In the dye and fragrance industry, Benzoic acid, 2,4-dihydroxy-5-nitro-, methyl ester (9CI) is used as a key intermediate in the production of various dyes and fragrances. Its unique chemical structure contributes to the color and scent profiles of these products, enhancing their performance and appeal.
Used in Antioxidant and Anti-inflammatory Applications:
Benzoic acid, 2,4-dihydroxy-5-nitro-, methyl ester (9CI) exhibits antioxidant and anti-inflammatory effects, making it a potential candidate for therapeutic applications in conditions such as cancer and inflammation. Its antioxidant properties can help neutralize harmful free radicals, while its anti-inflammatory effects can alleviate inflammation and reduce associated symptoms.
However, it is important to note that the toxicity and potential health hazards of Benzoic acid, 2,4-dihydroxy-5-nitro-, methyl ester (9CI) should be carefully considered and further studied before any widespread applications. Its mutagenicity and cytotoxic properties may pose risks to human health and the environment, necessitating thorough research and safety assessments.

Upstream product

• 89-86-1 4-hydroxysalicylic acid 
• 2150-47-2 methyl 2,4-dihydroxybenzoate 
• 67-56-1 methanol 
• 13722-96-8 2,4-dihydroxy-5-nitrobenzoic acid 

Downstream Products

• 271261-72-4 5-nitro-2,4-bis(octyloxy)benzoic acid methyl ester 
• 874210-15-8 2,4-bis{2-[2-(2-methoxyethoxy)ethoxy]ethoxy}-5-nitrobenzoic acid methyl ester 
• 874210-16-9 2,4-bis[3-(tert-butoxycarbonyl)propoxy]-5-nitrobenzoic acid methyl ester 
• 13722-96-8 2,4-dihydroxy-5-nitrobenzoic acid 
• 81574-75-6 2,4-dimethoxy-5-nitro-benzoic acid methyl ester 
• 271261-74-6 2,4-dimethoxy-5-nitro-benzoyl chloride 
• 271261-75-7 2,4-dioctyloxy-5-nitrobenzoyl chloride 
• 271261-76-8 3-(2,4-dioctyloxy-5-nitrobenzoylamino)-4-methoxytoluene 
• 271261-77-9 5-amino-N-(2-methoxy-5-methyl-phenyl)-2,4-bis-octyloxy-benzamide 
• 271261-78-0 3-(5-(2,4-dimethoxy-5-nitrobenzoylamino)-2,4-dioctyloxybenzoylamino)-4-methoxytoluene 
• 90564-41-3 2,4-dimethoxy-5-nitrobenzoic acid 
• 1383808-78-3 C₄₉H₈₀N₂O₉ 
• 1383808-80-7 C₄₈H₇₈N₂O₉ 
• 1383808-65-8 C₄₉H₈₂N₂O₇ 

Relevant academic research and scientific papers

An efficient entry to amino-substituted resorcylic acid derivatives for the synthesis of platensimycin and analogues

An efficient entry to protected amino-substituted resorcylic acid derivatives, methyl 3- or 5-amino-2,4-bis(methoxymethoxy)benzoate, is reported. Both derivatives can be used for the synthesis of platensimycin and its analogues. Georg Thieme Verlag Stuttg

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

IMMUNOMODULATORS, COMPOSITIONS AND METHODS THERE OF

Provided herein is compounds of Formula I, methods of using the compounds as immunomodulators, and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders such as cancer

IMMUNOMODULATORS, COMPOSITIONS AND METHODS THEREOF

Provided herein are compounds of Formula (I), methods of using the compounds as immunomodulators, and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders such as cancer or infections.

CAVITY-CONTAINING OLIGOMERS AND POLYMERS EFFECTIVE IN CRYOPRESERVATION

The present invention provides compositions and methods for cryopreservation utilizing aromatic cavity-containing oligomers and polymers that contain structural motifs capable of shape-inducing intramolecular bonding to form cavities. The cavity-containin

HETEROCYCLIC COMPOUNDS AS IMMUNOMODULATORS

Disclosed are compounds of Formula (I), methods of using the compounds as immunomodulators, and pharmaceutical compositions comprising such compounds. The compounds are useful in treating, preventing or ameliorating diseases or disorders such as cancer or

Synthesis of crescent aromatic oligoamides

This article describes the synthetic procedures for the preparation of crescent (and helical) aromatic oligoamides developed in recent years in our laboratory. The large-scale preparation of a variety of monomers derived from various tetrasubstituted benzenes is presented. Three different strategies for constructing various oligomers consisting of meta- and meta/para-linked benzene residues are discussed. Factors affecting coupling efficiency and yields are analyzed. The developed synthetic methods have provided the basis for the preparation of longer oligomers and for the development of solid-phase synthesis.