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2-(Furan-2-yl)pyrrolidine is a heterocyclic compound characterized by the fusion of a pyrrolidine ring with a furan ring attached to one of its nitrogen atoms. This unique molecular structure endows the compound with distinctive properties, positioning it as a valuable building block in the synthesis of pharmaceuticals and agrochemicals. Its versatility and potential applications across various fields, including chemistry, pharmaceuticals, and materials science, make it an attractive target for research and development.

90086-89-8

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90086-89-8 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
2-(Furan-2-yl)pyrrolidine is utilized as a key building block for the development of new pharmaceuticals and agrochemicals. Its presence in these compounds contributes to their unique properties and potential therapeutic or pesticidal effects.
Used in the Creation of Functional Materials:
Due to its structural features, 2-(Furan-2-yl)pyrrolidine is employed as a component in the design and synthesis of various functional materials, where its properties can be harnessed for specific applications.
Used as a Ligand in Metal-Catalyzed Reactions:
2-(Furan-2-yl)pyrrolidine has demonstrated its potential as a ligand in metal-catalyzed reactions, playing a crucial role in enhancing the efficiency and selectivity of these processes.
Used in Drug Discovery and Development:
2-(Furan-2-yl)pyrrolidine's interesting biological activities have made it a promising candidate for drug discovery and development, where it could be further optimized for therapeutic applications.

Check Digit Verification of cas no

The CAS Registry Mumber 90086-89-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,0,8 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 90086-89:
(7*9)+(6*0)+(5*0)+(4*8)+(3*6)+(2*8)+(1*9)=138
138 % 10 = 8
So 90086-89-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H11NO/c1-3-7(9-5-1)8-4-2-6-10-8/h2,4,6-7,9H,1,3,5H2

90086-89-8SDS

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 2-(Furan-2-yl)pyrrolidine

1.2 Other means of identification

Product number -
Other names 2-(FURAN-2-YL)PYRROLIDINE

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:90086-89-8 SDS

90086-89-8Relevant academic research and scientific papers

α-Functionalization of Cyclic Secondary Amines: Lewis Acid Promoted Addition of Organometallics to Transient Imines

Paul, Anirudra,Seidel, Daniel

supporting information, p. 8778 - 8782 (2019/06/07)

Cyclic imines, generated in situ from their corresponding N-lithiated amines and a ketone hydride acceptor, undergo reactions with a range of organometallic nucleophiles to generate α-functionalized amines in a single operation. Activation of the transient imines by Lewis acids that are compatible with the presence of lithium alkoxides was found to be crucial to accommodate a broad range of nucleophiles including lithium acetylides, Grignard reagents, and aryllithiums with attenuated reactivities.

A NOVEL THREE CARBON-AMINO GRIGNARD REAGENT: ITS USE IN AN EFFICIENT PYRROLIDINE SYNTHESIS

Basha, Fatima Z.,DeBernardis, John F.

, p. 5271 - 5274 (2007/10/02)

A novel primary amino protected Grignard reagent has been developed; 2,2,5,5-tetramethyl-1-aza-2,5-disilacyclopentane-1-propyl magnesium bromide 1a.Its usefulness is illustrated in the synthesis of 2-substituted pyrrolidines.

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