1352035-31-4 Usage
Molecular structure
A complex organic compound with a unique structure, containing a perfluorophenyl group, a triazolo ring, an oxazin ring, and a tetrafluoroborate anion.
Perfluorophenyl group
A phenyl ring with all hydrogen atoms replaced by fluorine atoms, which contributes to the compound's stability and chemical resistance.
Triazolo ring
A five-membered heterocyclic ring with three nitrogen atoms and two carbon atoms, which provides the compound with interesting chemical properties and potential reactivity.
Oxazin ring
A six-membered heterocyclic ring with one oxygen atom and one nitrogen atom, which contributes to the compound's structural diversity and potential applications in medicinal chemistry.
Tetrafluoroborate anion
A negatively charged ion with four fluorine atoms attached to a boron atom, which can act as a leaving group in chemical reactions and influence the compound's reactivity.
Potential applications
Due to its unique structure and properties, the compound has potential applications in organic synthesis, medicinal chemistry, and materials science.
Industrial sectors
Further research and development of this chemical could lead to new technologies and applications in various industrial sectors, such as pharmaceuticals, agrochemicals, and advanced materials.
Check Digit Verification of cas no
The CAS Registry Mumber 1352035-31-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,0,3 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1352035-31:
(9*1)+(8*3)+(7*5)+(6*2)+(5*0)+(4*3)+(3*5)+(2*3)+(1*1)=114
114 % 10 = 4
So 1352035-31-4 is a valid CAS Registry Number.
1352035-31-4Relevant articles and documents
Chemoselective N-heterocyclic carbene-catalyzed cross-benzoin reactions: Importance of the fused ring in triazolium salts
Langdon, Steven M.,Wilde, Myron M.D.,Thai, Karen,Gravel, Michel
supporting information, p. 7539 - 7542 (2014/06/10)
Morpholinone- and piperidinone-derived triazolium salts are shown to catalyze highly chemoselective cross-benzoin reactions between aliphatic and aromatic aldehydes. The reaction scope includes ortho-, meta-, and para-substituted benzaldehyde derivatives with a range of electron-donating and -withdrawing groups as well as branched and unbranched aliphatic aldehydes. Catalytic loadings as low as 5 mol % give excellent yields in these reactions (up to 99%).
