1028263-94-6 Usage
Uses
Used in Pharmaceutical Industry:
1-Fluoro-2-iodo-4-methoxybenzene is used as a chemical intermediate for the synthesis of various pharmaceuticals. Its unique structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agrochemical Industry:
In the agrochemical industry, 1-Fluoro-2-iodo-4-methoxybenzene serves as a key intermediate in the production of agrochemicals. Its properties contribute to the creation of effective pesticides, herbicides, and other agricultural chemicals.
Used in Materials Science:
1-Fluoro-2-iodo-4-methoxybenzene has potential applications in the field of materials science. Its unique structure and properties can be utilized in the development of new materials with specific characteristics, such as improved stability, reactivity, or other desirable properties.
Used as a Substrate in Chemical Reactions:
Due to its reactivity, 1-Fluoro-2-iodo-4-methoxybenzene can be used as a substrate in various chemical reactions. It can be further modified or transformed into other compounds, expanding its potential applications in organic synthesis and other chemical processes.
It is crucial to handle and use 1-fluoro-2-iodo-4-methoxybenzene with caution, as it may pose health risks and environmental hazards if mishandled. Proper safety measures and guidelines should be followed to ensure the safe use of this chemical compound in various applications.
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.
