252644-60-3 Usage
Chemical structure
A piperidine derivative with two 4-fluorophenyl substituents attached to the piperidine ring.
Application
Commonly used in organic synthesis and pharmaceutical research as a building block for the production of various drug candidates and bioactive molecules.
Usage in analytical chemistry
May be used as a reference standard in analytical chemistry and spectroscopy.
Unique properties
The presence of fluorine substituents on the phenyl rings can impart unique chemical and biological properties to this compound.
Potential for further investigation
Due to its unique properties, it is of interest for further investigation and potential application in drug development and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 252644-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,2,6,4 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 252644-60:
(8*2)+(7*5)+(6*2)+(5*6)+(4*4)+(3*4)+(2*6)+(1*0)=133
133 % 10 = 3
So 252644-60-3 is a valid CAS Registry Number.
252644-60-3Relevant articles and documents
Copper(I)-catalyzed coupling reaction of aryl boronic acids with N,O-acetals and N,N-aminals under atmosphere leading to α-aryl glycine derivatives and diarylmethylamine derivatives
Sakai, Norio,Hori, Hiroaki,Yoshida, Yoshihiro,Konakahara, Takeo,Ogiwara, Yohei
, p. 4722 - 4729 (2015/07/27)
We demonstrated a copper(I)-catalyzed coupling reaction of aryl boronic acids with N,O-acetals and N,N-aminals leading to the synthesis of α-aryl glycines and diarylmethylamines. Under an ambient atmosphere, this catalytic system could be applied to the activation of a C(sp3)-O bond of N,O-acetals with an ester and an aryl group, or without a coordinating substituent, as well as to a C(sp3)-N bond of N,N-aminals.