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(1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid is a complex carboxylic acid derivative featuring a cyclopentane ring fused with a pyrrole ring. This unique molecular structure suggests potential reactivity and interactions with biological systems, indicating possible pharmaceutical or biological relevance. Its carboxylic acid group provides functionalization, allowing for further chemical modifications and reactions. Further research is necessary to explore the full scope of its properties and applications.

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  • 926276-11-1 Structure
  • Basic information

    1. Product Name: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid
    2. Synonyms: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid
    3. CAS NO:926276-11-1
    4. Molecular Formula: C8H13NO2
    5. Molecular Weight: 155
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 926276-11-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 304℃
    3. Flash Point: 138℃
    4. Appearance: /
    5. Density: 1.182
    6. Refractive Index: N/A
    7. Storage Temp.: 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(926276-11-1)
    11. EPA Substance Registry System: (1S,3aR,6aS)-Octahydrocyclopenta[c]pyrrole-1-carboxylic acid(926276-11-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 926276-11-1(Hazardous Substances Data)

926276-11-1 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.

Check Digit Verification of cas no

The CAS Registry Mumber 926276-11-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,6,2,7 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 926276-11:
(8*9)+(7*2)+(6*6)+(5*2)+(4*7)+(3*6)+(2*1)+(1*1)=181
181 % 10 = 1
So 926276-11-1 is a valid CAS Registry Number.

926276-11-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1S,3aR,6aS)-octahydrocyclopenta[c]pyrrole-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names (1S,3aR,6aS)-octahydro cyclopenta[c]pyrrole-1- carboxylic acid

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:926276-11-1 SDS

926276-11-1Relevant articles and documents

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

Reddy, G. Sudhakar,Reddy, D. Srinivas,Corey

supporting information, p. 2258 - 2262 (2021/04/05)

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

-

, (2014/04/17)

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

Koehler, Valentin,Bailey, Kevin R.,Znabet, Anass,Raftery, James,Helliwell, Madeleine,Turner, Nicholas J.

supporting information; experimental part, p. 2182 - 2184 (2010/06/18)

"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.

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