274674-23-6 Usage
Description
(S)-(-)-2-(Fluorodiphenylmethyl)pyrrolidine is a chiral compound that features a pyrrolidine ring and a fluorodiphenylmethyl group. It is widely recognized for its use as a building block in organic synthesis, particularly within the pharmaceutical industry for the development of various chiral drugs. (S)-(-)-2-(FLUORODIPHENYLMETHYL)PYRROLI& has demonstrated potent biological activities, such as antiviral and antitumor properties, positioning it as a promising candidate for drug development. Additionally, its chiral nature renders it a valuable asset in asymmetric synthesis and catalysis, contributing to its versatility and broad applicability across different sectors.
Uses
Used in Pharmaceutical Industry:
(S)-(-)-2-(Fluorodiphenylmethyl)pyrrolidine is used as a building block for the synthesis of chiral drugs, leveraging its unique structure and properties to create medications with improved efficacy and selectivity.
Used in Antiviral Applications:
(S)-(-)-2-(FLUORODIPHENYLMETHYL)PYRROLI& serves as an antiviral agent, exhibiting potent biological activities against various viral pathogens. Its development into antiviral drugs could potentially offer new treatment options for a range of viral infections.
Used in Antitumor Applications:
(S)-(-)-2-(Fluorodiphenylmethyl)pyrrolidine is utilized as an antitumor agent, thanks to its demonstrated ability to combat tumor growth. Its integration into cancer treatment strategies may lead to the development of novel therapeutic approaches for various types of cancer.
Used in Asymmetric Synthesis:
The chiral nature of (S)-(-)-2-(Fluorodiphenylmethyl)pyrrolidine makes it an essential component in asymmetric synthesis, a technique that allows for the creation of specific enantiomers of chiral molecules with high selectivity. This application is crucial in the production of enantiomerically pure compounds, which are often essential for the desired biological activity of drugs.
Used in Catalysis:
This versatile compound is also employed in catalysis, where its chiral properties can be harnessed to enhance the efficiency and selectivity of various chemical reactions. Its use in catalytic processes can lead to improved synthetic routes and the development of more environmentally friendly and cost-effective methods in the chemical and pharmaceutical industries.
Check Digit Verification of cas no
The CAS Registry Mumber 274674-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,4,6,7 and 4 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 274674-23:
(8*2)+(7*7)+(6*4)+(5*6)+(4*7)+(3*4)+(2*2)+(1*3)=166
166 % 10 = 6
So 274674-23-6 is a valid CAS Registry Number.
274674-23-6Relevant articles and documents
A concise synthesis of (S)-2-(fluorodiphenylmethyl)pyrrolidine: A novel organocatalyst for the stereoselective epoxidation of α,β-unsaturated aldehydes
Sparr, Christof,Tanzer, Eva-Maria,Bachmann, Julia,Gilmour, Ryan
experimental part, p. 1394 - 1397 (2010/07/02)
A concise synthesis of (S)-2-(fluorodiphenylmethyl)pyrrolidine from cheap, commercially available starting materials is described. Pertinent features of this synthetic route include ease of synthesis, facile purification steps, and an operationally simple deoxy?fluorination step to install the C-F bond. Georg Thieme Verlag Stuttgart · New York.
PROCESS FOR PREPARING CHIRAL COMPOUNDS
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Page/Page column 7, (2008/06/13)
Process for the preparation of chiral compounds of formula (I) comprising contacting a compound of formula (II) with a source of hydrogen or halide; wherein A is a chiral center; X is selected from oxygen, sulphur and nitrogen; n is selected from 0 and 1
