CAS 2900-63-2

3,5-Dinitrobenzoic acid hydrazide

Description:

3,5-Dinitrobenzoic acid hydrazide is an organic compound characterized by its hydrazide functional group attached to a dinitrobenzoic acid moiety. It typically appears as a crystalline solid and is known for its yellow to orange coloration. The presence of two nitro groups on the benzene ring significantly influences its chemical reactivity and properties, making it a potent electrophile. This compound is often utilized in organic synthesis and as an intermediate in the preparation of various pharmaceuticals and agrochemicals. Its hydrazide functionality allows for the formation of hydrazones and other derivatives, which are valuable in medicinal chemistry. Additionally, 3,5-dinitrobenzoic acid hydrazide exhibits moderate solubility in polar solvents, which can facilitate its use in various chemical reactions. Safety precautions should be observed when handling this compound, as nitro compounds can be hazardous and may pose environmental risks. Overall, its unique structure and reactivity make it a significant compound in chemical research and applications.

Formula: C₇H₆N₄O₅

InChI: InChI=1/C7H6N4O5/c8-9-7(12)4-1-5(10(13)14)3-6(2-4)11(15)16/h1-3H,8H2,(H,9,12)

InChI key: InChIKey=IJVPILVRNBBRSO-UHFFFAOYSA-N

SMILES: C(NN)(=O)C1=CC(N(=O)=O)=CC(N(=O)=O)=C1

Synonyms:

• 3,5-Dinitrobenzhydrazide
• 3,5-Dinitrobenzenecarboxylic acid hydrazide
• Benzoic acid, 3,5-dinitro-, hydrazide
• 3,5-Dinitrobenzoic acid hydrazide
• 3,5-Dinitrobenzoylhydrazine
• 3,5-Dinitrobenzohydrazide
• 3,5-DINITRO-BENZOIC ACID HYDRAZIDE
• Einecs 220-790-2

3,5-Dinitrobenzohydrazide

CAS: 2900-63-2

Formula: C₇H₆N₄O₅

Purity: 98%

Molecular weight: 226.1463

Ref: IN-DA002V6Y

3,5-Dinitrobenzohydrazide

CAS: 2900-63-2

3,5-Dinitrobenzohydrazide

Purity: 98%

Molecular weight: 226.15g/mol

Ref: 54-OR1036475

3,5-Dinitrobenzhydrazide

CAS: 2900-63-2

3,5-Dinitrobenzhydrazide (DNBBH) is a chemical compound that is used as an anticancer agent. It has been shown to be effective in treating autoimmune diseases by inhibiting the production of aldehydes and reactive oxygen species, which causes oxidative stress in the body. DNBBH can be synthesized by refluxing 3,5-dinitrobenzoic acid with benzhydrazide. The resulting product can be purified by recrystallization from ethanol. This synthesis may also produce some impurities, such as 2-nitrobenzoic acid or 2-nitrodiphenylamine. These impurities are removed through recrystallization from chloroform or ether.
2,4-Dinitrophenol (DNP) can also be used for the synthesis of DNBBH by refluxing DNP with benzhydrazide under acidic conditions. This synthesis produces more than one molecule of

Formula: C₇H₆N₄O₅

Purity: Min. 95%

Color and Shape: Powder

Molecular weight: 226.15 g/mol

Ref: 3D-FD70500

3,5-Dinitrobenzohydrazide

CAS: 2900-63-2

Purity: 98%

Molecular weight: 226.147995

Ref: 10-F642303