37535-43-6
2-Methyl-chinolin-6-carbonsaeure-amide
CAS: 37535-43-6
Molecular Formula: C11H10N2O
37535-43-6 - Names and Identifiers
| Name | 2-Methyl-chinolin-6-carbonsaeure-amide |
| Synonyms | 2-Methylquinoline-6-carboxamide 2-Methyl-chinolin-6-carbonsaeure-aMid 2-Methyl-chinolin-6-carbonsaeure-amide |
| CAS | 37535-43-6 |
37535-43-6 - Physico-chemical Properties
| Molecular Formula | C11H10N2O |
| Molar Mass | 186.21 |
37535-43-6 - Introduction
The chemical structure is C11H10N2O, which is an organic compound. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: White crystalline solid.
-Solubility: Soluble in ethanol, chloroform and dichloromethane, slightly soluble in water.
Use:
-It can be used as an organic synthesis intermediate, and is commonly used in the fields of drug synthesis and pesticide synthesis.
Preparation Method: The preparation of
-phosphor can be obtained from the reaction of 2-methylquinoline and formyl chloride. The specific preparation method includes dissolving 2-methyl quinoline in an organic solvent, then adding formyl chloride for reaction, and finally obtaining the compound by crystallization or extraction.
Safety Information:
-It is less harmful, but it is still necessary to pay attention to the stimulating effect it may bring during operation.
-During use or storage, care should be taken to avoid contact with oxidants and strong acids.
-During operation, you should wear appropriate personal protective equipment, such as gloves and goggles.
-If the substance is inhaled or touched by mistake, the affected area should be cleaned immediately and medical help should be sought.
Nature:
-Appearance: White crystalline solid.
-Solubility: Soluble in ethanol, chloroform and dichloromethane, slightly soluble in water.
Use:
-It can be used as an organic synthesis intermediate, and is commonly used in the fields of drug synthesis and pesticide synthesis.
Preparation Method: The preparation of
-phosphor can be obtained from the reaction of 2-methylquinoline and formyl chloride. The specific preparation method includes dissolving 2-methyl quinoline in an organic solvent, then adding formyl chloride for reaction, and finally obtaining the compound by crystallization or extraction.
Safety Information:
-It is less harmful, but it is still necessary to pay attention to the stimulating effect it may bring during operation.
-During use or storage, care should be taken to avoid contact with oxidants and strong acids.
-During operation, you should wear appropriate personal protective equipment, such as gloves and goggles.
-If the substance is inhaled or touched by mistake, the affected area should be cleaned immediately and medical help should be sought.
Last Update：2024-04-09 19:05:50
