1-(chloroacetyl)pyrrolidine
1-(chloroacetyl)pyrrolidine
CAS: 20266-00-6
Molecular Formula: C6H10ClNO
1-(chloroacetyl)pyrrolidine - Names and Identifiers
| Name | 1-(chloroacetyl)pyrrolidine |
| Synonyms | AI3-36314 AKOS BBS-00000922 TIMTEC-BB SBB005370 ASINEX-REAG BAS 12710677 1-(Chloroacetyl)pyrrolidine 1-(chloroacetyl)pyrrolidine 1-(CHLOROACETYL)PYRROLIDINE Pyrrolidine, 1-(chloroacetyl)- 2-CHLORO-1-PYRROLIDIN-1-YL-ETHANONE 2-chloro-1-(pyrrolidin-1-yl)ethanone Pyrrolidine, 1-(chloroacetyl)- (6CI,7CI,8CI,9CI) |
| CAS | 20266-00-6 |
| EINECS | 243-658-6 |
| InChI | InChI=1/C6H10ClNO/c7-5-6(9)8-3-1-2-4-8/h1-5H2 |
| InChIKey | AAOSLLBWWRKJIR-UHFFFAOYSA-N |
1-(chloroacetyl)pyrrolidine - Physico-chemical Properties
| Molecular Formula | C6H10ClNO |
| Molar Mass | 147.6 |
| Density | 1.205±0.06 g/cm3(Predicted) |
| Melting Point | 46-47°C |
| Boling Point | 105°C/1.3mmHg(lit.) |
| Flash Point | 106.8°C |
| Vapor Presure | 0.0188mmHg at 25°C |
| pKa | -0.95±0.20(Predicted) |
| Storage Condition | Room Temprature |
| Refractive Index | 1.501 |
1-(chloroacetyl)pyrrolidine - Risk and Safety
| Hazard Symbols | Xn - Harmful |
| Risk Codes | R22 - Harmful if swallowed R20/21/22 - Harmful by inhalation, in contact with skin and if swallowed. |
| Safety Description | S23 - Do not breathe vapour. S24/25 - Avoid contact with skin and eyes. |
| WGK Germany | 3 |
| HS Code | 29339900 |
| Hazard Class | IRRITANT |
1-(chloroacetyl)pyrrolidine - Introduction
1-(chloroacetyl)pyrrolidine is an organic compound with the molecular formula C6H10ClNO and the structural formula ClCH2CO-NH-C4H7. The following is a description of its nature, use, preparation and safety information:
Nature:
1-(chloroacetyl)pyrrolidine is a colorless liquid with a pungent odor. It can be dissolved in many organic solvents, such as alcohols, ethers and esters. It is almost insoluble in water.
Use:
1-(chloroacetyl)pyrrolidine is used as an important synthetic intermediate in organic synthesis. It can be used to synthesize drugs, dyes, pesticides and other organic compounds. It is commonly used in the pharmaceutical field for the preparation of amide compounds.
Method:
1-(chloroacetyl)pyrrolidine has many preparation methods, and the common methods include the following two:
1. The tetrahydropyrrole and chloroacetic acid are esterified in a chemical reaction to generate the target product.
2. chloroacetyl chloride is reacted with tetrahydropyrrole under alkaline conditions to generate 1-(chloroacetyl)pyrrolidine.
Safety Information:
1-(chloroacetyl)pyrrolidine needs to be safe when using and storing. It is irritating, so avoid inhaling its vapor and skin contact during operation. Also, follow Good Laboratory Practices and wear appropriate protective equipment such as goggles, gloves and lab clothes. When handling this compound, local laws and regulations and operating guidelines should be followed.
Nature:
1-(chloroacetyl)pyrrolidine is a colorless liquid with a pungent odor. It can be dissolved in many organic solvents, such as alcohols, ethers and esters. It is almost insoluble in water.
Use:
1-(chloroacetyl)pyrrolidine is used as an important synthetic intermediate in organic synthesis. It can be used to synthesize drugs, dyes, pesticides and other organic compounds. It is commonly used in the pharmaceutical field for the preparation of amide compounds.
Method:
1-(chloroacetyl)pyrrolidine has many preparation methods, and the common methods include the following two:
1. The tetrahydropyrrole and chloroacetic acid are esterified in a chemical reaction to generate the target product.
2. chloroacetyl chloride is reacted with tetrahydropyrrole under alkaline conditions to generate 1-(chloroacetyl)pyrrolidine.
Safety Information:
1-(chloroacetyl)pyrrolidine needs to be safe when using and storing. It is irritating, so avoid inhaling its vapor and skin contact during operation. Also, follow Good Laboratory Practices and wear appropriate protective equipment such as goggles, gloves and lab clothes. When handling this compound, local laws and regulations and operating guidelines should be followed.
Last Update：2024-04-09 21:11:58
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