Cis-Octahydro-cyclopenta(c)pyrrole - Names and Identifiers
Name | octahydrocyclopenta[c]pyrrole
|
Synonyms | Gliclazide Impurity 13 3-Azabicyclo[3.3.0]octane 1,3-Azabicyclo[3.3.0]octane Octahydrocyclopenta(c)pyrrole octahydrocyclopenta[c]pyrrole Cyclopenta[c]pyrrole,octahydro- octahydrocyclopenta[c]pyrrole HCL Cis-Octahydro-cyclopenta(c)pyrrole N-Amino-3-azabicyclo[3.3.0]hydrochloride 1,2,3,3a,4,5,6,6a-octahydrocyclopenta[c]pyrrole
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CAS | 5661-03-0
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EINECS | 227-114-5 |
InChI | InChI=1/C7H13N/c1-2-6-4-8-5-7(6)3-1/h6-8H,1-5H2 |
Cis-Octahydro-cyclopenta(c)pyrrole - Physico-chemical Properties
Molecular Formula | C7H13N
|
Molar Mass | 111.18 |
Density | 0.934±0.06 g/cm3(Predicted) |
Boling Point | 165.0±8.0 °C(Predicted) |
Flash Point | 44.8°C |
Water Solubility | 1000g/L at 20℃ |
Vapor Presure | 8.1hPa at 20℃ |
pKa | 11.53±0.20(Predicted) |
Storage Condition | 2-8°C(protect from light) |
Refractive Index | 1.478 |
Cis-Octahydro-cyclopenta(c)pyrrole - Introduction
octahydrocyclopenta[c]pyrrole, also known as octahydrocyclopenta[c]pyrrole, is an organic compound. Its chemical formula is C9H15N, and its structure has a five-membered ring and an imidazole ring. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: octahydrocyclopenta[c]pyrrole is a colorless to pale yellow liquid.
-Solubility: It is soluble in many organic solvents, such as ethanol, dimethylformamide and dichloromethane.
-Stability: The compound is relatively stable under conventional conditions, but may decompose under high temperature, high pressure or light.
Use:
-Chemical synthesis: octahydrocyclopenta[c]pyrrole can be used as intermediates in organic synthesis reactions and can be used to synthesize some biologically active compounds.
-Drug research: It also has certain applications in the field of drug research, and can be used as a ligand or building block of certain drugs.
Preparation Method:
octahydrocyclopenta[c] There are many preparation methods of pyrrole, and one of the more commonly used methods is synthesis by cyclization reaction of imidazole ring. Specific steps are as follows:
1. Taking benzaldehyde and ethyl acetate as raw materials, Michael addition reaction was carried out in an appropriate solvent to generate N-phenylmethacrylamide.
2. The imidazole ring is synthesized under basic conditions to obtain the octahydrocyclopenta[c]pyrrole.
Safety Information:
-When handling or storing octahydrocyclopenta[c]pyrrole, take care to avoid contact with skin, eyes and respiratory tract to prevent irritation and injury.
-When using this compound, follow laboratory safety procedures and wear appropriate protective equipment such as gloves, glasses and laboratory coats.
-If contact or aspiration occurs, immediately flush the affected area with clean water and seek medical help.
-This information only provides basic safety guidance. Please consult the relevant laboratory and chemical safety information before the experiment, and follow the correct safety operation.
Last Update:2024-04-09 15:17:58