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203059-85-2

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203059-85-2 Usage

General Description

1,2-Diiodo-4-fluorobenzene is a chemical compound with the molecular formula C6H3I2F. It is a halogenated aromatic compound that is used in various chemical reactions and organic synthesis processes. 1,2-Diiodo-4-fluorobenzene is a derivative of benzene, with two iodine atoms and one fluorine atom attached to the benzene ring. 1,2-Diiodo-4-fluorobenzene is known for its reactivity as a versatile building block in organic chemistry, particularly in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It is also used as a reagent in cross-coupling reactions and other carbon-carbon bond forming processes. Overall, 1,2-Diiodo-4-fluorobenzene is an important chemical intermediate with a range of applications in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 203059-85-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,3,0,5 and 9 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 203059-85:
(8*2)+(7*0)+(6*3)+(5*0)+(4*5)+(3*9)+(2*8)+(1*5)=102
102 % 10 = 2
So 203059-85-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H3FI2/c7-4-1-2-5(8)6(9)3-4/h1-3H

203059-85-2Relevant articles and documents

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.

supporting information, p. 15617 - 15628 (2016/12/16)

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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