1050666-51-7

Basic information

• Product Name: 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione
• Synonyms: 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione
• CAS NO: 1050666-51-7
• Molecular Formula: C7H10N2O2
• Molecular Weight: 154.1665
• Mol File: 1050666-51-7.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione(1050666-51-7)
• EPA Substance Registry System: 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione(1050666-51-7)

Safety Data

• Hazardous Substances Data: 1050666-51-7(Hazardous Substances Data)

Usage

General Description

2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione is a chemical compound with a complex and specific molecular structure. It is a cyclic compound that contains nitrogen and oxygen atoms, and it is also known as a pyrrolopyrrole. 2-aMinotetrahydro-Cyclopenta[c]pyrrole-1,3(2H,3aH)-dione has potential applications in fields such as pharmaceuticals and materials science due to its unique structure and properties. It may have biological activity and may be used in the development of new drugs or materials. Its precise synthesis and characterization are essential for understanding its potential uses and effects.

Upstream product

• 5763-44-0 4,5,6,6a-tetrahydro-3aH-cyclopenta[c]pyrrole-1,3-dione 

Relevant articles and documents

Synthesis process of N-amino-3-azabicyclo [3, 3, 0] octane hydrochloride

The invention provides a synthesis process of N-amino-3-azabicyclo [3, 3, 0] octane hydrochloride, and relates to the technical field of gliclazide intermediate synthesis. The synthesis process comprises the following steps: heating, dehydrating and cyclizing 2-carbamoyl amine cyclopentanecarboxylate serving as a raw material under the catalysis of an acid catalyst until no water is generated, adding toluene, refluxing and dissolving, and carrying out post-treatment to obtain 1, 2-cyclopentane dicarboximide; reacting the 1, 2-cyclopentane dicarboximide with chloramine under an alkaline condition, and carrying out post-treatment to obtain N-amino-1, 2-cyclopentane dicarboximide; and reducing the amino-1, 2-cyclopentane dicarboximide in the presence of sodium borohydride/aluminum trichloride and an organic solvent, and performing post-treatment to obtain the product. According to the present invention, the three-step synthesis is performed through the catalytic cyclization reaction, the nucleophilic substitution reaction and the reduction reaction, the raw materials are cheap and easily available, the high toxicity product is not generated, the harsh reaction condition is not required, the yield and the purity of each step are high, and the method is suitable for the large-scale industrial production.