352535-00-3 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-(+)-2-(Fluorodiphenylmethyl)pyrroli& is used as a key building block for the development of various pharmaceuticals. Its unique structural properties and chiral nature contribute to the creation of novel drugs with improved efficacy and selectivity.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (R)-(+)-2-(Fluorodiphenylmethyl)pyrroli& is utilized for the synthesis of compounds with potential therapeutic applications. Its structural diversity and chirality enable the development of drugs that can target specific biological pathways, leading to more effective treatments.
Used in Asymmetric Synthesis Processes:
(R)-(+)-2-(Fluorodiphenylmethyl)pyrroli& is employed as a crucial component in asymmetric synthesis, where the stereochemistry of the molecule is critical for the desired chemical reactions. Its chiral nature allows for the creation of enantiomerically pure compounds, which are essential in various chemical and pharmaceutical applications.
Used in Chemical Compound Development:
(R)-(+)-2-(Fluorodiphenylmethyl)pyrroli& is also used in the development of new chemical compounds with potential applications in various industries. Its unique structural properties and chirality make it a versatile compound for exploring new chemical reactions and creating novel products.
Check Digit Verification of cas no
The CAS Registry Mumber 352535-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 352535-00:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*0)+(1*0)=123
123 % 10 = 3
So 352535-00-3 is a valid CAS Registry Number.
InChI:InChI=1/C17H18FN/c18-17(16-12-7-13-19-16,14-8-3-1-4-9-14)15-10-5-2-6-11-15/h1-6,8-11,16,19H,7,12-13H2/t16-/m1/s1
352535-00-3Relevant academic research and scientific papers
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.
