274674-23-6 Usage
General Description
The chemical (S)-(-)-2-(fluorodiphenylmethyl)pyrrolidine is a chiral compound that consists of a pyrrolidine ring and a fluorodiphenylmethyl group. It is commonly used as a building block in organic synthesis, particularly in the pharmaceutical industry for the preparation of various chiral drugs. (S)-(-)-2-(FLUORODIPHENYLMETHYL)PYRROLI& has been found to exhibit potent biological activities, including antiviral and antitumor properties, making it a valuable candidate for drug development. Its chiral nature also makes it useful in asymmetric synthesis and catalysis. Overall, (S)-(-)-2-(fluorodiphenylmethyl)pyrrolidine is a versatile chemical with significant potential for use in various industrial and medicinal applications.
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
