1H-Benzimidazole-1-acetic acid, 2-methyl-, hydrazide
2-(2-Methyl-1H-benzimidazol-1-yl)acetohydrazide
CAS: 97420-40-1
Molecular Formula: C10H12N4O
1H-Benzimidazole-1-acetic acid, 2-methyl-, hydrazide - Names and Identifiers
1H-Benzimidazole-1-acetic acid, 2-methyl-, hydrazide - Physico-chemical Properties
| Molecular Formula | C10H12N4O |
| Molar Mass | 204.23 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD00227235 |
1H-Benzimidazole-1-acetic acid, 2-methyl-, hydrazide - Introduction
2-(2-Methyl-benzimidazol-1-yl) acetohydrazide (2-(1-H) acetohydrazide) is an organic compound. It has a molecular formula of C11H13N5O and a molecular weight of 235.26g/mol.
Nature:
2-(2-Methyl-1H-benzimidazol-1-yl) acetohydrazide is a colorless crystalline solid. It is stable at room temperature and soluble in solvents.
Use:
2-(2-Methyl-1H-benzimidazol-1-yl) acetohydrazide is commonly used as an intermediate in the fields of medicine and organic synthesis. It can be used for the synthesis of novel chelating ligands, organic dyes and chemical fluorescent probes. In addition, it also has biological activities such as inhibition of metalloproteinase activity and anti-tumor activity.
Preparation Method:
2-(2-methyl-1H-benzimidazol-1-yl) acetohydrazide can be synthesized by acetylation of hydrazine. The specific step is that hydrazine is reacted with 2-methyl -1H-benzimidazol-1-one to generate 2-(2-methyl -1H-benzimidazol-1-yl) ethanone hydrazine, followed by an acylation reaction in acetic acid to obtain the target product.
Safety Information:
Due to the lack of relevant toxicological studies, the safety and potential hazards of 2-(2-methyl-1H-benzimidazol-1-yl) acetohydrazide are not clear. When using this compound, follow laboratory safety practices and avoid contact with skin, eyes, or inhalation of its gases or dust. If accidental exposure occurs, rinse immediately with plenty of water and seek medical help.
Nature:
2-(2-Methyl-1H-benzimidazol-1-yl) acetohydrazide is a colorless crystalline solid. It is stable at room temperature and soluble in solvents.
Use:
2-(2-Methyl-1H-benzimidazol-1-yl) acetohydrazide is commonly used as an intermediate in the fields of medicine and organic synthesis. It can be used for the synthesis of novel chelating ligands, organic dyes and chemical fluorescent probes. In addition, it also has biological activities such as inhibition of metalloproteinase activity and anti-tumor activity.
Preparation Method:
2-(2-methyl-1H-benzimidazol-1-yl) acetohydrazide can be synthesized by acetylation of hydrazine. The specific step is that hydrazine is reacted with 2-methyl -1H-benzimidazol-1-one to generate 2-(2-methyl -1H-benzimidazol-1-yl) ethanone hydrazine, followed by an acylation reaction in acetic acid to obtain the target product.
Safety Information:
Due to the lack of relevant toxicological studies, the safety and potential hazards of 2-(2-methyl-1H-benzimidazol-1-yl) acetohydrazide are not clear. When using this compound, follow laboratory safety practices and avoid contact with skin, eyes, or inhalation of its gases or dust. If accidental exposure occurs, rinse immediately with plenty of water and seek medical help.
Last Update：2024-04-09 20:52:54
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1H-Benzimidazole-1-acetic acid, 2-methyl-, hydrazide
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Thieno[3,2-c]pyridine-5(4H)-acetic acid, α-(2-chlorophenyl)-6,7-dihydro-2,3-bis(hydroxymethyl)-, methyl ester, (αS)-
sodium [4-[(4,5-dihydro-3-methyl-5-oxo-1-phenyl-1H-pyrazol-4-yl)azo]-3-hydroxynaphthalene-1-sulphonato(3-)]hydroxychromate(1-)