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Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione
[CAS# 5763-44-0]

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Complete supplier list of Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione
Identification
Classification Organic raw materials >> Heterocyclic compound >> Pyrroles
Name Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione
Synonyms 4,5,6,6a-tetrahydro-3aH-cyclopenta[c]pyrrole-1,3-dione
Molecular Structure CAS # 5763-44-0, Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione, 4,5,6,6a-tetrahydro-3aH-cyclopenta[c]pyrrole-1,3-dione
Molecular Formula C7H9NO2
Molecular Weight 139.15
CAS Registry Number 5763-44-0
EC Number 227-285-6
SMILES C1CC2C(C1)C(=O)NC2=O
Properties
Solubility Sparingly soluble (17 g/L) (25 ºC), Calc.*
Density 1.242±0.06 g/cm3 (20 ºC 760 Torr), Calc.*
Melting point 90 ºC**
Index of Refraction 1.518, Calc.*
Boiling Point 322.2±11.0 ºC (760 mmHg), Calc.*
Flash Point 162.2±19.4 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software V11.02 (©1994-2018 ACD/Labs)
** Menon, Kottiazath N.; Journal of the Chemical Society 1929, P302-5.
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H302-H312-H315-H317-H318-H319-H335-H412    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P272-P273-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P330-P332+P317-P333+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Eye irritationEye Irrit.2AH319
SDS Available
up Discovory and Applicatios
Tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione is a bicyclic compound characterized by its unique fused ring structure. This chemical substance, often simply referred to as a pyrrole derivative, has garnered interest in the field of organic chemistry due to its intriguing structural features and potential applications in various domains.

The discovery of tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione can be traced back to the exploration of pyrrole derivatives in the mid-20th century. Researchers were focused on synthesizing compounds with unique heterocyclic frameworks, which could exhibit interesting chemical and biological properties. The synthesis typically involves the cyclization of appropriate precursors, leading to the formation of the bicyclic structure. Several methods have been developed to achieve this, often focusing on the use of catalytic systems and selective reaction conditions to enhance yield and purity.

One of the significant applications of tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione lies in its role as an intermediate in the synthesis of pharmaceuticals. Due to its structural resemblance to naturally occurring compounds, it has been investigated for potential bioactivity, including antitumor and anti-inflammatory effects. The presence of the dione functional groups makes it a versatile precursor for further modifications, enabling the design of more complex pharmacologically active molecules.

In addition to its pharmaceutical potential, tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione has also found applications in materials science. Its unique structure can contribute to the development of new polymers and functional materials with specific properties, such as enhanced thermal stability and mechanical strength. This aspect is particularly relevant in the context of advanced material design, where the incorporation of heterocyclic compounds can lead to improved performance characteristics in various applications, including coatings and composites.

Research has also highlighted the potential of this compound in organic electronic materials. The unique electronic properties associated with its structure may facilitate the development of organic semiconductors or photovoltaic materials, paving the way for advancements in renewable energy technologies. The ability to fine-tune the properties of tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione through chemical modifications makes it an attractive candidate for exploration in these fields.

Ongoing studies aim to explore the full spectrum of applications for tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione, including its mechanisms of action in biological systems and its interactions with other chemical compounds. Researchers continue to investigate novel synthetic approaches to improve yield and reduce environmental impact, reflecting a growing emphasis on sustainable practices in chemical research.

In conclusion, tetrahydrocyclopenta[c]pyrrole-1,3(2H,3aH)-dione represents a significant chemical substance with diverse applications in pharmaceuticals and materials science. Its discovery and exploration underline the importance of heterocyclic compounds in advancing both scientific knowledge and practical applications in various fields.
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