2-Methyl-4,5,6,7-tetrahydro-2H-indazole-3-carboxylic acid - Names and Identifiers
Name | 2-Methyl-4,5,6,7-tetrahydro-2H-indazole-3-carboxylic acid
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Synonyms | 2-methyl-4,5,6,7-tetrahydroindazole-3-carboxylic acid 2-Methyl-4,5,6,7-tetrahydro-2H-indazole-3-carboxylic acid 2H-Indazole-3-carboxylic acid, 4,5,6,7-tetrahydro-2-methyl-
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CAS | 32287-00-6
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2-Methyl-4,5,6,7-tetrahydro-2H-indazole-3-carboxylic acid - Physico-chemical Properties
Molecular Formula | C9H12N2O2
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Molar Mass | 180.2 |
Density | 1.39±0.1 g/cm3(Predicted) |
Melting Point | 205.6 °C |
Boling Point | 378.2±42.0 °C(Predicted) |
pKa | 0.63±0.20(Predicted) |
Storage Condition | Room Temprature |
Sensitive | Irritant |
MDL | MFCD04092072 |
2-Methyl-4,5,6,7-tetrahydro-2H-indazole-3-carboxylic acid - Introduction
2-methyl -4,5,6, 7-tetrahydro-2H-indazole-3-carboxylic acid is an organic compound with the chemical formula C9H11NO2. It is a white solid, soluble in some organic solvents such as chloroform and dichloromethane. The following is a detailed description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: White solid
-melting point: about 115-117 ℃
-Boiling Point: No data
-Solubility: Soluble in some organic solvents such as chloroform and dichloromethane, insoluble in water
-Molecular weight: 165.19g/mol
Use:
2-Methyl -4,5,6, 7-tetrahydro-2H-indazole-3-carboxylic acid is an intermediate compound with multiple applications in the field of drug development:
-Drug synthesis: It can be used as an intermediate for the preparation of antibacterial drugs, anti-tumor drugs and other biologically active compounds.
-Chemical research: It can be used in reactions in organic chemical synthesis, such as the synthesis of various organic compounds.
-Laboratory research: It can be used to prepare compounds for different purposes, such as catalysts, ligands and other organometallic compounds.
Preparation Method:
2-Methyl -4,5,6, 7-tetrahydro-2H-indazole-3-carboxylic acid can be synthesized by a variety of methods. A common synthesis method is generated by the reaction of indazole:
-Indazole synthesis: First, under appropriate conditions, the N-atom of indazole is methylated, and then it is carboxylated under basic conditions.
Safety Information:
2-Methyl -4,5,6, 7-tetrahydro-2H-indazole-3-carboxylic acid has limited safety and toxicity information. As an organic compound, it may have certain toxicity and irritation, so safety measures need to be paid attention to when handling and storing. When in use, it is recommended to wear appropriate protective equipment, such as gloves and goggles, to avoid direct contact with skin and eyes. In a laboratory environment, regulations and safe operating procedures for the use of relevant chemicals should be observed. Be aware of and follow relevant safety education and guidance before performing any chemical experiments. If necessary, it is recommended to consult a laboratory safety expert or a senior chemist.
Last Update:2024-04-09 21:01:54