1476776-56-3 Usage
Structure
It is a cyclic ketone with a tetrahydro-2H-pyran ring and a 4-bromophenyl group attached.
Potential Applications
Organic synthesis
Medicinal chemistry
Utility as a Building Block
Synthesis of pharmaceuticals
Synthesis of other organic compounds
Biological Activity
Presence of bromophenyl group suggests potential biological activity
Research Interest
Interest in further investigation and research due to its unique structure and potential biological activity.
Check Digit Verification of cas no
The CAS Registry Mumber 1476776-56-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,7,6,7,7 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1476776-56:
(9*1)+(8*4)+(7*7)+(6*6)+(5*7)+(4*7)+(3*6)+(2*5)+(1*6)=223
223 % 10 = 3
So 1476776-56-3 is a valid CAS Registry Number.
1476776-56-3Relevant articles and documents
Regio- and enantioselective Baeyer-Villiger oxidation: Kinetic resolution of racemic 2-substituted cyclopentanones
Zhou, Lin,Liu, Xiaohua,Ji, Jie,Zhang, Yuheng,Wu, Wangbin,Liu, Yangbin,Lin, Lili,Feng, Xiaoming
supporting information, p. 3938 - 3941 (2014/08/18)
A kinetic resolution of racemic 2-substituted cyclopentanones via highly regio- and enantioselective Baeyer-Villiger oxidation has been successfully developed. The reaction could afford the normal 6-substituted δ-lactones in up to 98% ee and >19/1 regioselectivity. Meanwhile, the unreacted ketones were recovered in excellent ee values (up to 98%). It represents the best results of the kinetic resolution of racemic 2-substituted cyclopentanones via nonenzymic asymmetric BV oxidation.
