(3aR,6aS)-hexahydro-1H-furo[3,4-c]pyrrole
1H-Furo[3,4-c]pyrrole, hexahydro-, cis-
CAS: 55129-05-0
Molecular Formula: C6H11NO
(3aR,6aS)-hexahydro-1H-furo[3,4-c]pyrrole - Names and Identifiers
(3aR,6aS)-hexahydro-1H-furo[3,4-c]pyrrole - Physico-chemical Properties
| Molecular Formula | C6H11NO |
| Molar Mass | 113.16 |
| Density | 1.028±0.06 g/cm3(Predicted) |
| Boling Point | 177.9±33.0 °C(Predicted) |
| pKa | 10.54±0.20(Predicted) |
| Storage Condition | 2-8°C(protect from light) |
(3aR,6aS)-hexahydro-1H-furo[3,4-c]pyrrole - Introduction
1H-Furo[3,4-c]pyrrole, hexahydro-, cis-(1H-Furo[3,4-c]pyrrole, hexahydro-, cis-), abbreviated as 1H-Furo[3,4-c]pyrrole. The following is a description of its nature, use, preparation and safety information:
Nature:
1H-Furo[3,4-c]pyrrole is an organic compound with a molecular formula of C9H13NO and a molecular weight of 151.2g/mol. It is a solid with a pale yellow to tan crystalline form. It has a unique aroma. The compound is relatively stable at room temperature and pressure.
Use:
1H-Furo[3,4-c]pyrrole has a wide range of applications in organic chemistry. It is an important intermediate for the preparation of pyrrole derivatives, furan derivatives and other organic synthetic target compounds. In addition, it can also be used as dyes, catalysts and active ingredients in the pharmaceutical field.
Preparation Method:
1H-Furo[3,4-c]pyrrole can be synthesized by a variety of methods. The commonly used method is to cyclize pyrrole and furan to generate the target compound. In the reaction process, it is usually necessary to use an acidic catalyst and an appropriate solvent to control the reaction conditions and improve the yield.
Safety Information:
Limited safety information regarding the 1H-Furo[3,4-c]pyrrole. Because the toxicity and safety of the compounds have not been extensively studied, care should be taken in their use and handling. It is recommended to wear appropriate protective equipment, such as lab gloves and safety glasses, when performing experimental operations. In addition, avoid inhaling its dust or vapor, and ensure that the operation is carried out in a well-ventilated place. If you are exposed to or ingested by a compound, you should seek medical advice immediately and bring information about the compound.
Nature:
1H-Furo[3,4-c]pyrrole is an organic compound with a molecular formula of C9H13NO and a molecular weight of 151.2g/mol. It is a solid with a pale yellow to tan crystalline form. It has a unique aroma. The compound is relatively stable at room temperature and pressure.
Use:
1H-Furo[3,4-c]pyrrole has a wide range of applications in organic chemistry. It is an important intermediate for the preparation of pyrrole derivatives, furan derivatives and other organic synthetic target compounds. In addition, it can also be used as dyes, catalysts and active ingredients in the pharmaceutical field.
Preparation Method:
1H-Furo[3,4-c]pyrrole can be synthesized by a variety of methods. The commonly used method is to cyclize pyrrole and furan to generate the target compound. In the reaction process, it is usually necessary to use an acidic catalyst and an appropriate solvent to control the reaction conditions and improve the yield.
Safety Information:
Limited safety information regarding the 1H-Furo[3,4-c]pyrrole. Because the toxicity and safety of the compounds have not been extensively studied, care should be taken in their use and handling. It is recommended to wear appropriate protective equipment, such as lab gloves and safety glasses, when performing experimental operations. In addition, avoid inhaling its dust or vapor, and ensure that the operation is carried out in a well-ventilated place. If you are exposed to or ingested by a compound, you should seek medical advice immediately and bring information about the compound.
Last Update：2024-04-09 21:54:55
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Product Name: Syringaresinol Impurity 5 Visit Supplier Webpage Request for quotationCAS: 55129-05-0
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Product Name: (3aR,6aS)-rel-hexahydro-1H-Furo[3,4-c]pyrrole (Relative struc) Visit Supplier Webpage Request for quotation
CAS: 55129-05-0
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CAS: 55129-05-0
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