1365565-32-7 Usage
Structure
A pyran-4(3H)-one derivative with a phenylvinyl substituent at the 2-position
Usage
Often used in organic synthesis and medicinal chemistry as a building block for constructing more complex molecules
Unique value
Its unique structure and reactivity make it valuable for developing new pharmaceuticals and materials
Potential applications
May have potential applications in the development of novel dyes and agrochemicals due to its aromatic nature and functional groups.
Check Digit Verification of cas no
The CAS Registry Mumber 1365565-32-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,5,5,6 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1365565-32:
(9*1)+(8*3)+(7*6)+(6*5)+(5*5)+(4*6)+(3*5)+(2*3)+(1*2)=177
177 % 10 = 7
So 1365565-32-7 is a valid CAS Registry Number.
1365565-32-7Relevant academic research and scientific papers
Competitive [2,3]-and [1,2]-oxonium ylide rearrangements. Concerted or stepwise?
Jaber, Deana M.,Burgin, Ryan N.,Helper, Matthew,Zavalij, Peter Y.,Doyle, Michael P.
supporting information; experimental part, p. 1676 - 1679 (2012/06/30)
The axial-equatorial conformational isomer distribution of the reactant diazoacetoacetate or its metal carbene intermediate is reflected in Rh(II) catalyzed oxonium ylide forming reactions of 3-(trans-2-arylvinyl) tetrahydropyranone-5-diazoacetoacetates that afford diastereoisomeric products for both the symmetry-allowed [2,3]-and the formally symmetry-forbidden [1,2]-oxonium ylide rearrangements.
