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4-chloro-1,2-bis(tetrafluoropyridinylethynyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

459457-32-0

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459457-32-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 459457-32-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,4,5 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 459457-32:
(8*4)+(7*5)+(6*9)+(5*4)+(4*5)+(3*7)+(2*3)+(1*2)=190
190 % 10 = 0
So 459457-32-0 is a valid CAS Registry Number.

459457-32-0Upstream product

459457-32-0Downstream Products

459457-32-0Relevant academic research and scientific papers

Orbital Crossings Activated through Electron Injection: Opening Communication between Orthogonal Orbitals in Anionic C1-C5 Cyclizations of Enediynes

Peterson, Paul W.,Shevchenko, Nikolay,Breiner, Boris,Manoharan, Mariappan,Lufti, Forat,Delaune, Jess,Kingsley, Margaret,Kovnir, Kirill,Alabugin, Igor V.

, p. 15617 - 15628 (2016)

Generally, the long-range electronic communication between spatially orthogonal orbitals is inefficient and limited to field and inductive effects. In this work, we provide experimental evidence that such communication can be achieved via intramolecular electron transfer between two degenerate and mutually orthogonal frontier molecular orbitals (MOs) at the transition state. Interaction between orthogonal orbitals is amplified when the energy gap between these orbitals approaches zero, or at an “orbital crossing”. The crossing between two empty or two fully occupied MOs, which do not lead to stabilization, can be “activated” when one of the empty MOs is populated (i.e., electron injection) or one of the filled MOs is depopulated (i.e., hole injection). In reductive cycloaromatization reactions, such crossings define transition states with energies defined by both the in-plane and out-of-plane π-systems. Herein, we provide experimental evidence for the utility of this concept using orbital crossings in reductive C1-C5 cycloaromatization reactions of enediynes. Communication with remote substituents via orbital crossings greatly enhances regioselectivity of the ring closure step in comparison to the analogous radical cyclizations. We also present photophysical data pertaining to the efficiency of electron injection into the benzannelated enediynes.

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