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(3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole is a heterocyclic chemical compound with the molecular formula C10H15NO2. It is a derivative of pyrrolopyrrole, featuring a six-membered ring with nitrogen and a five-membered ring with nitrogen. Characterized by the presence of an ethoxycarbonyl group, which is a carbonyl group attached to an ethoxy group, (3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole plays a significant role in organic synthesis and medicinal chemistry.

1114985-14-6

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1114985-14-6 Usage

Uses

Used in Organic Synthesis:
(3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole is used as a building block in organic synthesis for the preparation of various pharmaceuticals and bioactive compounds. Its unique structure and functional groups make it a valuable component in the creation of new molecules with potential therapeutic properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole is utilized as a key intermediate for the synthesis of pharmaceuticals. Its ability to form stable complexes with biological targets allows for the development of drugs with improved efficacy and selectivity.
Used in Materials Science:
(3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole may have potential applications in materials science. It can be employed in the development of organic semiconductors, where its electronic properties can be harnessed for use in electronic devices. Additionally, it may serve as a ligand in coordination chemistry, contributing to the formation of metal complexes with specific properties for various applications.
Used in the Development of Organic Semiconductors:
In the application industry of organic semiconductors, (3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole is used as a component for designing and synthesizing new semiconductor materials. Its incorporation into these materials can enhance their electronic properties, making them suitable for use in various electronic devices such as solar cells, transistors, and light-emitting diodes.
Used as a Ligand in Coordination Chemistry:
In the coordination chemistry application industry, (3aS,6aS)-5-Ethoxycarbonyl-1H-hexahydropyrrolo[3,4-b]pyrrole is used as a ligand to form metal complexes. Its coordination with metal ions can result in complexes with unique properties, which can be applied in areas such as catalysis, sensing, and drug design.

Check Digit Verification of cas no

The CAS Registry Mumber 1114985-14-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,1,4,9,8 and 5 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1114985-14:
(9*1)+(8*1)+(7*1)+(6*4)+(5*9)+(4*8)+(3*5)+(2*1)+(1*4)=146
146 % 10 = 6
So 1114985-14-6 is a valid CAS Registry Number.

1114985-14-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl (3aS,6aS)-2,3,3a,4,6,6a-hexahydro-1H-pyrrolo[2,3-c]pyrrole-5-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:1114985-14-6 SDS

1114985-14-6Relevant academic research and scientific papers

The identification of pyrimidine-diazabicyclo[3.3.0]octane derivatives as 5-HT2C receptor agonists

Huck, Bayard R.,Llamas, Luis,Robarge, Michael J.,Dent, Thomas C.,Song, Jianping,Hodnick, William F.,Crumrine, Chris,Stricker-Krongrad, Alain,Harrington, John,Brunden, Kurt R.,Bennani, Youssef L.

, p. 2891 - 2894 (2006)

The 5-HT2C receptor has been implicated in the regulation of appetite. As such, small molecule agonists to this receptor may serve as novel therapies to combat obesity. We describe here the identification, synthesis, and SAR of a 5-HT2C/s

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