61429-10-5 Usage
Structure
Derivative of butanoic acid with a methyl group at the third carbon and a pyrrole ring at the second carbon.
Aromaticity
Presence of the pyrrole ring confers aromatic character to the compound.
Chemical Properties
Unique properties due to the presence of the pyrrole ring.
Applications
Commonly used in pharmaceutical research and development.
Functionality
Potential for targeting specific biological pathways and receptors.
Utility
Synthesis of new drugs and medications.
Biological Impact
Can modulate biological processes and interactions in the body.
Check Digit Verification of cas no
The CAS Registry Mumber 61429-10-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,2 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 61429-10:
(7*6)+(6*1)+(5*4)+(4*2)+(3*9)+(2*1)+(1*0)=105
105 % 10 = 5
So 61429-10-5 is a valid CAS Registry Number.
61429-10-5Relevant academic research and scientific papers
Enantioselective Synthesis of N-Benzylic Heterocycles: A Nickel and Photoredox Dual Catalysis Approach
Pezzetta, Cristofer,Bonifazi, Davide,Davidson, Robert W. M.
supporting information, p. 8957 - 8961 (2019/11/11)
Reported herein is a dual nickel- and photoredox-catalyzed modular approach for the preparation of enantioenriched N-benzylic heterocycles. α-Heterocyclic carboxylic acids, easily obtainable from common commercial material, are reported as suitable substrates for a decarboxylative strategy in conjunction with a chiral pyridine-oxazoline (PyOx) ligand, providing quick access to enantioenriched drug-like products. The presence of a directing group on the heterocyclic moiety is shown to be beneficial, affording improved stereoselectivity in a number of cases.
