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Atomfair m-Aminobenzohydrazide C7H9N3O
Description m-Aminobenzohydrazide (CAS No. 14062-34-1) is a high-purity organic compound with the molecular formula C7H9N3O , widely utilized in pharmaceutical and chemical research. This white to off-white crystalline powder is characterized by its hydrazide functional group and aromatic amine substitution at the meta position, making it a versatile intermediate in synthetic chemistry. With a molecular weight of 151.17 g/mol, it offers excellent solubility in polar organic solvents such as DMSO and methanol, facilitating its use in diverse reaction conditions. Our product undergoes rigorous quality control, including HPLC and NMR analysis, to ensure ??98% purity, meeting the stringent requirements of research…
Description
Description
m-Aminobenzohydrazide (CAS No. 14062-34-1) is a high-purity organic compound with the molecular formula C7H9N3O, widely utilized in pharmaceutical and chemical research. This white to off-white crystalline powder is characterized by its hydrazide functional group and aromatic amine substitution at the meta position, making it a versatile intermediate in synthetic chemistry. With a molecular weight of 151.17 g/mol, it offers excellent solubility in polar organic solvents such as DMSO and methanol, facilitating its use in diverse reaction conditions. Our product undergoes rigorous quality control, including HPLC and NMR analysis, to ensure ??98% purity, meeting the stringent requirements of research laboratories and industrial applications. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability and prevent degradation.
- CAS No: 14062-34-1
- Molecular Formula: C7H9N3O
- Molecular Weight: 151.17
- Exact Mass: 151.074561919
- Monoisotopic Mass: 151.074561919
- IUPAC Name: 3-aminobenzohydrazide
- SMILES: C1=CC(=CC(=C1)N)C(=O)NN
- Synonyms: m-Aminobenzohydrazide, 3-Aminobenzhydrazide, 14062-34-1, 3-Aminobenzohydrazide, Benzoic acid, 3-amino-, hydrazide
Application
m-Aminobenzohydrazide serves as a key building block in the synthesis of heterocyclic compounds, particularly in the development of pharmaceuticals and agrochemicals. It is employed in the preparation of hydrazone derivatives, which exhibit potential biological activities such as antimicrobial and anticancer properties. Researchers also utilize this compound in the design of Schiff base ligands for coordination chemistry and catalysis. Its reactive amino and hydrazide groups enable facile conjugation with carbonyl compounds, making it valuable in combinatorial chemistry and drug discovery.
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