Benzoic acid, 5-hydroxy-2,4-dinitro-

Base Information

• Chemical Name: Benzoic acid, 5-hydroxy-2,4-dinitro-
• CAS No.: 54797-73-8
• Molecular Formula: C7H4N2O7
• Molecular Weight: 228.118
• Mol file: 54797-73-8.mol

Synonyms:

Chemical Property of Benzoic acid, 5-hydroxy-2,4-dinitro-

Chemical Property:

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Use Description: Benzoic acid, 5-hydroxy-2,4-dinitro-, is a chemical compound with applications in various fields. In the field of organic synthesis, it serves as a valuable intermediate for the creation of complex organic molecules, especially in the pharmaceutical and agrochemical industries. Its unique chemical structure allows for the introduction of specific functional groups and structural motifs into target molecules, making it an essential building block for the development of therapeutic agents, dyes, and specialty chemicals. Its role is fundamental in advancing chemical synthesis and the production of compounds with potential clinical or industrial applications. Additionally, in the field of explosives and propellants, this compound can find utility as an ingredient in the formulation of explosives, where its explosive properties contribute to the controlled release of energy. Its significance in this context lies in its role in pyrotechnics and the production of explosives used for various industrial, military, and entertainment purposes. While its significance varies within these fields, it consistently plays a pivotal role in advancing chemical synthesis, drug development, and explosive materials across diverse scientific and industrial applications.

Technology Process of Benzoic acid, 5-hydroxy-2,4-dinitro-

There total 14 articles about Benzoic acid, 5-hydroxy-2,4-dinitro- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 50.0%

3-Carboxyphenol (99-06-9) → 5-hydroxy-2-nitrobenzoic acid (610-37-7) + 3-hydroxy-4-nitro-benzoic acid (619-14-7) + 5-hydroxy-2,4-dinitrobenzoic acid (54797-73-8) + 3-hydroxy-2,6-dinitrobenzoic acid (67175-28-4)

Guidance literature:

With ammonium cerium(IV) nitrate; In acetonitrile; at 20 ℃; for 12h;

DOI:10.1002/jccs.200500086

Reference yield:

3-Carboxyphenol (99-06-9) → 5-hydroxy-2,4-dinitrobenzoic acid (54797-73-8) + 3-hydroxy-2,4-dinitro-benzoic acid (116779-73-8)

Guidance literature:

With nitric acid; at 50 - 60 ℃; Reinigung ueber das Blei(II)-Salz;

Reference yield:

2,4,5-trinitro-benzoic acid (29235-52-7) → 5-hydroxy-2,4-dinitrobenzoic acid (54797-73-8)

Guidance literature:

With sodium carbonate;

upstream raw materials:

1-methyl-4-nitrosobenzene

2,4,5-trinitro-benzoic acid

5-fluoro-2,4-dinitro-benzoic acid

5-chloro-2,4-dinitrobenzoic acid

Downstream raw materials:

3-hydroxy-2,4,6-trinitro-benzoic acid

Refernces