115705-50-5

Basic information

• Product Name: 1,4-Benzenedicarboxylic acid, 2-amino-5-nitro-
• CAS NO: 115705-50-5
• Molecular Formula: C8H6N2O6
• Molecular Weight: 226.145
• Mol File: 115705-50-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1,4-Benzenedicarboxylic acid, 2-amino-5-nitro-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Benzenedicarboxylic acid, 2-amino-5-nitro-(115705-50-5)
• EPA Substance Registry System: 1,4-Benzenedicarboxylic acid, 2-amino-5-nitro-(115705-50-5)

Safety Data

• Hazardous Substances Data: 115705-50-5(Hazardous Substances Data)

Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is an alternative name for the compound, which is derived from its parent compound, terephthalic acid.

Explanation

The compound is derived from terephthalic acid, which is a precursor in the synthesis of various polymers and chemicals.

Explanation

The compound is used as a building block in the synthesis of various organic compounds, which are then used in the production of pharmaceuticals, dyes, and pigments.

Explanation

The compound has the ability to form coordination complexes with metal ions, which can be useful in various chemical and industrial applications.

Explanation

Research has been conducted on the compound's potential anticancer and antibacterial properties, which could lead to its use in the development of new drugs and treatments.

Explanation

The compound's structure consists of a benzene ring with a 2-amino group, a 5-nitro group, and two carboxylic acid groups attached to the 1 and 4 positions. This structure contributes to its various properties and applications.

Derivative of

Terephthalic acid

Applications

Pharmaceutical, dye, and pigment production

Coordination complexes

Forms with metal ions

Potential properties

Anticancer and antibacterial

Chemical structure

Contains a benzene ring, amino group, nitro group, and two carboxylic acid groups

Upstream product

• 1134102-20-7 dimethyl 2-[(ethoxycarbonyl)amino]-5-nitroterephthalate 
• 177284-13-8 dimethyl-2-acetamido-5-nitroterephthalate 
• 5441-05-4 dimethyl acetamidoterephthalate 
• 115705-49-2 2-formamidoterephthalic acid 
• 10312-55-7 3-aminoterephthalic acid 
• 610-29-7 2-nitroterephthalic acid 
• 177284-15-0 dimethyl 2-amino-5-nitroterephthalate 

Downstream Products

• 945-30-2 2,5-diaminoterephthalic acid 
• 115705-53-8 2,5-diacetamido-3-nitroterephthalic acid dimethyl ester 

Relevant articles and documents

Aromatic Substituent Effects on the Flexibility of Metal-Organic Frameworks

The flexibility (or breathing behavior) of zinc-based metal-organic frameworks (MOFs) has been manipulated by regioisomeric and positional control of organic functionalities. Ten new regioisomeric BDC (ortho- or para-disubstituted benzene-1,4-dicarboxylic

Synthesis and Electrochemistry of Pyrimidoquinazoline-5,10-diones. Design of Hydrolytically Stable High Potential Quinones and New Reductive Alkylation Systems

The synthesis of pyrimidoquinazoline-5,10-diones 1 and pyrimidoquinazoline-5,10-diones 2 was carried out in conjunction with the design of both hydrolytically stable high potential quinones and new purine-like reductive alkylators.These systems consist of a benzoquinone ring bearing two fused pyrimidin-4(3H)-one rings.The fused pyrimidinone rings serve to protect 1 and 2 from hydrolysis as well as to raise quinone redox potentials by stabilizing the hydroquinones with internal hydrogen bonds (65 mV increase per hydrogen bond).Synthesis of 1 and 2 involved pyrimidinone ring annelation to a 2,5-diamino-3-nitroterephthalic acid derivative and to a 2,4-diamino-1,5-dicarboxy-3-nitrobenzene derivative, respectively.The synthetic studies provided insights into the electronic effects of nitro and amino groups on the annelation process.

Azo dyestuffs

Azo dyestuffs, which in the acid form, are represented by the formula: wherein A is an aromatic radical, M is a 1,4-benzene radical which may be substituted, E is the residue of a coupling component which is free from azo groups, At least one of A and M containing a phosphonic acid group, and the metal complexes of those having a metallisable group are reactive dyes suitable for use in the process of German OLS No. 2324809.