926276-11-1

Basic information

• Product Name: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid
• Synonyms: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid
• CAS NO: 926276-11-1
• Molecular Formula: C8H13NO2
• Molecular Weight: 155
• Mol File: 926276-11-1.mol

Chemical Properties

• Boiling Point: 304℃
• Flash Point: 138℃
• Appearance: /
• Density: 1.182
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(926276-11-1)
• EPA Substance Registry System: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(926276-11-1)

Safety Data

• Hazardous Substances Data: 926276-11-1(Hazardous Substances Data)

Usage

Uses

Given the provided materials, there are no specific applications listed for (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid. However, based on its chemical characteristics, we can hypothesize potential uses in various industries:
Used in Pharmaceutical Industry:
(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid could be used as a pharmaceutical intermediate for the synthesis of bioactive compounds due to its complex molecular structure and functional groups, which may allow for interactions with biological targets.
Used in Chemical Research:
In the field of chemical research, (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid may serve as a subject for studying the reactivity of carboxylic acid derivatives fused with heterocyclic rings, potentially leading to the discovery of new reaction pathways or mechanisms.
Used in Material Science:
(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid might also be explored in material science for its potential to form novel materials with unique properties, such as polymers or coordination complexes, owing to its ability to participate in various chemical reactions.

Upstream product

• 926276-09-7 C₁₃H₂₁NO₄ 
• 1205676-37-4 (1S,3aR,6aS)-octahydrocyclopenta[c]pyrrole-1-carbonitrile 
• 6140-65-4 1-cyclopentene-1-carboxaldehyde 
• 1414976-22-9 C₉H₁₅NO₄ 
• 629-11-8 1,6-hexanediol 
• 1292320-79-6 (1R,2R)-2-(nitromethyl)cyclopentane-1-carbaldehyde 
• 1037834-39-1 (3aR,6aS)-octahydrocyclopenta[c]pyrrole 
• 1114553-80-8 (E)-7-nitrohept-6-enal 
• 110-83-8 cyclohexene 
• 55489-11-7 6,6-dimethoxyhexanal 
• 1227703-50-5 octahydrocyclopenta[c]pyrrole-1-carbonitrile 
• 1227703-21-0 (3aR,6aS)-1,3a,4,5,6,6a-hexahydrocyclopenta[c]pyrrole 
• 1414976-36-5 C₁₅H₁₉NO₂ 
• 1414976-28-5 C₁₆H₂₃NO₂ 

Downstream Products

• 714194-68-0 tert-butyl (1S,3aR,6aS)-octahydrocyclopenta[c]pyrrole-1-carboxylate 
• 597569-42-1 (1S,3aR,6aS)-2-(tert-butoxycarbonyl)octahydrocyclo-penta[c]pyrrole-1-carboxylic acid 

Relevant articles and documents

Unraveling the C2-Symmetric Azatetraquinane System. Simple, Enantioselective Syntheses

Concise stereocontrolled synthetic routes to the C2-symmetric azatetraquinane 1 (or, also, the enantiomer) are described. The successful execution of the synthesis involved innovation in the methodology for [3+2] cycloaddition and stereochemical control.

PROCESS FOR PRODUCING ESTER COMPOUND

Compound (1) or a salt that is useful as an intermediate for the production of a medicine, an agrochemical or the like can be produced by a process including the following steps: (A) reacting an aldehyde (2) with nitromethane to produce a nitroaldehyde; (B) reacting the nitroaldehyde with an alcohol to produce a nitroacetal; (C) reducing the nitroacetal to produce an aminoacetal; (D) protecting an amino group in the aminoacetal to produce a protected aminoacetal; (E) treating the protected aminoacetal with an acid and subsequently with a base and then reacting the resultant product with a cyanating agent to produce a nitrile; (F) hydrolyzing the nitrile to produce a protected amino acid; and (G) substituting a group R5 in the protected amino acid by a hydrogen atom and protecting a carboxyl group therein.

Enantioselective biocatalytic oxidative desymmetrization of substituted pyrrolidines

"Chemical Equation Presented" Center stage: Additions of nitrogen-centered radicals to cyanamide compounds provided the first radical synthesis of aromatic polycyclic guanidine derivatives (see scheme). Modular assembly of the substrates allows for a rapid increase of the molecular complexity of scaffolds, which have potential applications for medicinal chemistry.