5-(4-METHOXYPHENYL)PYRROLO (2,1-D)*(1,5) BENZOTHIAZ
5-(4-METHOXYPHENYL)PYRROLO[2,1-D][1,5]BENZOTHIAZEPIN-4-OL N,N-DIMETHYLCARBAMATE
CAS: 131403-82-2
Molecular Formula: C22H20N2O3S
5-(4-METHOXYPHENYL)PYRROLO (2,1-D)*(1,5) BENZOTHIAZ - Names and Identifiers
5-(4-METHOXYPHENYL)PYRROLO (2,1-D)*(1,5) BENZOTHIAZ - Physico-chemical Properties
| Molecular Formula | C22H20N2O3S |
| Molar Mass | 392.47 |
| Appearance | Off-white solid. |
| Storage Condition | 2-8°C |
| Physical and Chemical Properties | Storage Conditions: 2-8 ℃ WGK Germany:3 |
5-(4-METHOXYPHENYL)PYRROLO (2,1-D)*(1,5) BENZOTHIAZ - Risk and Safety
| Hazard Symbols | Xi - Irritant |
| Risk Codes | 36/37/38 - Irritating to eyes, respiratory system and skin. |
| Safety Description | S26 - In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. S36 - Wear suitable protective clothing. |
| WGK Germany | 3 |
5-(4-METHOXYPHENYL)PYRROLO (2,1-D)*(1,5) BENZOTHIAZ - Introduction
5-(4-Methoxyphenyl) pyrrole [2,1-D][1,5] benzothiepin-4-ol-N, N-dimethylcarbamate is an organic compound. The following is a description of its nature, use, preparation and safety information:
Nature:
-Appearance: A colorless or pale yellow solid.
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
-Molecular structure: It is a compound containing pyrrole, benzothiepine and methoxyphenyl functional groups.
Use:
-Chemical synthesis: 5-(4-methoxyphenyl) pyrrole [2,1-D][1,5] benzothiepine-4-ol-N, N-dimethylcarbamate can be used as an intermediate in organic synthesis for the preparation of other compounds.
-Optical material: Because its molecular structure contains benzothiepine and pyrrole, it has certain optical properties, so it can be used to prepare optical materials.
Preparation Method:
The preparation method of this compound is relatively complicated, and it generally needs to be synthesized through a multi-step reaction. The specific preparation method will vary according to the specific literature and experimental conditions.
Safety Information:
-The specific toxicity and danger of the compound are not clear, so it is necessary to strictly abide by the safe operation specifications of chemical experiments when using and handling the compound.
-Wear appropriate personal protective equipment such as lab gloves, goggles and lab coats during operation.
-Avoid contact with skin, eyes or inhalation. If you accidentally touch, rinse immediately with plenty of water.
-When using and storing the compound, the relevant laws and regulations should be observed to ensure safe use.
Nature:
-Appearance: A colorless or pale yellow solid.
-Solubility: Soluble in some organic solvents, such as dimethyl sulfoxide and dimethylformamide.
-Molecular structure: It is a compound containing pyrrole, benzothiepine and methoxyphenyl functional groups.
Use:
-Chemical synthesis: 5-(4-methoxyphenyl) pyrrole [2,1-D][1,5] benzothiepine-4-ol-N, N-dimethylcarbamate can be used as an intermediate in organic synthesis for the preparation of other compounds.
-Optical material: Because its molecular structure contains benzothiepine and pyrrole, it has certain optical properties, so it can be used to prepare optical materials.
Preparation Method:
The preparation method of this compound is relatively complicated, and it generally needs to be synthesized through a multi-step reaction. The specific preparation method will vary according to the specific literature and experimental conditions.
Safety Information:
-The specific toxicity and danger of the compound are not clear, so it is necessary to strictly abide by the safe operation specifications of chemical experiments when using and handling the compound.
-Wear appropriate personal protective equipment such as lab gloves, goggles and lab coats during operation.
-Avoid contact with skin, eyes or inhalation. If you accidentally touch, rinse immediately with plenty of water.
-When using and storing the compound, the relevant laws and regulations should be observed to ensure safe use.
Last Update：2024-04-09 21:04:16
