TIMTEC-BB SBB011056
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde
CAS: 151409-82-4
Molecular Formula: C12H13NO2
TIMTEC-BB SBB011056 - Names and Identifiers
TIMTEC-BB SBB011056 - Physico-chemical Properties
| Molecular Formula | C12H13NO2 |
| Molar Mass | 203.24 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD03924689 |
TIMTEC-BB SBB011056 - Risk and Safety
| Risk Codes | 22 - Harmful if swallowed |
| Hazard Class | IRRITANT |
TIMTEC-BB SBB011056 - Introduction
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde, also known as 1-(2-methoxyethyl)-1H-indole-3-carbaldehyde, is an organic compound. Its molecular formula is C13H13NO2 and its relative molecular mass is 215.25.
Nature:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde is a yellow to orange crystal with a distinctive odor. It is soluble in many organic solvents, such as ethanol, dimethylthionamide and dichloromethane.
Use:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde has many applications in the field of organic synthesis. It is an important intermediate for the synthesis of various compounds containing indole structures, such as drugs, pesticides and other biologically active molecules. It can also be used in the preparation of flavors and fragrances.
Preparation Method:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde can be synthesized by the basic reaction of indole. One common method of preparation is by reacting the indole with a formaldehyde or carbinol acetaldehyde acylating agent.
Safety Information:
When operating 1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde, follow the relevant safety procedures. It may be irritating to the eyes and skin and direct contact should be avoided. During use, inhalation or ingestion should be avoided. It is recommended to operate in a well-ventilated environment and wear appropriate protective gloves and glasses. Appropriate protective clothing should be worn if necessary. If inhaled or ingested, seek medical attention immediately.
Nature:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde is a yellow to orange crystal with a distinctive odor. It is soluble in many organic solvents, such as ethanol, dimethylthionamide and dichloromethane.
Use:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde has many applications in the field of organic synthesis. It is an important intermediate for the synthesis of various compounds containing indole structures, such as drugs, pesticides and other biologically active molecules. It can also be used in the preparation of flavors and fragrances.
Preparation Method:
1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde can be synthesized by the basic reaction of indole. One common method of preparation is by reacting the indole with a formaldehyde or carbinol acetaldehyde acylating agent.
Safety Information:
When operating 1-(2-Methoxy-ethyl)-1H-indole-3-carbaldehyde, follow the relevant safety procedures. It may be irritating to the eyes and skin and direct contact should be avoided. During use, inhalation or ingestion should be avoided. It is recommended to operate in a well-ventilated environment and wear appropriate protective gloves and glasses. Appropriate protective clothing should be worn if necessary. If inhaled or ingested, seek medical attention immediately.
Last Update：2024-04-09 15:18:10
