1028263-94-6 Usage
General Description
1-Fluoro-2-iodo-4-methoxybenzene is a chemical compound with the molecular formula C7H6FIO. It is a halogenated aromatic compound with a fluorine atom, an iodine atom, and a methoxy group attached to a benzene ring. This chemical is commonly used as an intermediate in organic synthesis and can be utilized in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It may also have potential applications in the field of materials science and as a substrate in various chemical reactions. Due to its unique structure and reactivity, 1-fluoro-2-iodo-4-methoxybenzene has garnered interest in the scientific community for its potential in developing new chemical processes and materials. However, it is important to handle and use this compound with caution, as it may pose health risks and environmental hazards if mishandled.
Check Digit Verification of cas no
The CAS Registry Mumber 1028263-94-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,2,6 and 3 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1028263-94:
(9*1)+(8*0)+(7*2)+(6*8)+(5*2)+(4*6)+(3*3)+(2*9)+(1*4)=136
136 % 10 = 6
So 1028263-94-6 is a valid CAS Registry Number.
1028263-94-6Relevant articles and documents
Utilising Sodium-Mediated Ferration for Regioselective Functionalisation of Fluoroarenes via C?H and C?F Bond Activations
Maddock, Lewis C. H.,Nixon, Tracy,Kennedy, Alan R.,Probert, Michael R.,Clegg, William,Hevia, Eva
, p. 187 - 191 (2018)
Pairing iron bis(amide) Fe(HMDS)2 with Na(HMDS) to form new sodium ferrate base [(dioxane)0.5?NaFe(HMDS)3] (1) enables regioselective mono and di-ferration (via direct Fe?H exchange) of a wide range of fluoroaromatic substrates under mild reaction conditions. Trapping of several ferrated intermediates has provided key insight into how synchronised Na/Fe cooperation operates in these transformations. Furthermore, using excess 1 at 80 °C switches on a remarkable cascade process inducing the collective twofold C?H/threefold C?F bond activations, where each C?H bond is transformed to a C?Fe bond whereas each C?F bond is transformed into a C?N bond.
