289039-23-2 Usage
Description
2-bromo-4-ethyl-1-iodobenzene is a halogenated aromatic compound with the molecular formula C8H8BrI. It is a derivative of benzene, featuring a bromine atom at the 2-position, an ethyl group at the 4-position, and an iodine atom at the 1-position on the benzene ring. This unique structure and reactivity make it a valuable building block in organic synthesis and pharmaceutical research.
Uses
Used in Organic Synthesis:
2-bromo-4-ethyl-1-iodobenzene is used as a building block for the synthesis of various organic compounds. Its reactivity allows for the modification and functionalization of other organic molecules, making it a versatile component in the creation of new chemical entities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-bromo-4-ethyl-1-iodobenzene is utilized as a key intermediate in the development of new drugs. Its unique structure contributes to the design and synthesis of potential therapeutic agents, aiding in the advancement of medicinal chemistry.
Used in Material Science:
2-bromo-4-ethyl-1-iodobenzene also has potential applications in material science. Its properties can be harnessed in the development of new materials with specific characteristics, such as improved stability or enhanced functional properties, for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 289039-23-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,9,0,3 and 9 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 289039-23:
(8*2)+(7*8)+(6*9)+(5*0)+(4*3)+(3*9)+(2*2)+(1*3)=172
172 % 10 = 2
So 289039-23-2 is a valid CAS Registry Number.
289039-23-2Relevant articles and documents
The Multiple Facets of Iodine(III) Compounds in an Unprecedented Catalytic Auto-amination for Chiral Amine Synthesis
Buendia, Julien,Grelier, Gwendal,Darses, Benjamin,Jarvis, Amanda G.,Taran, Frédéric,Dauban, Philippe
supporting information, p. 7530 - 7533 (2016/07/06)
Iodine(III) reagents are used in catalytic one-pot reactions, first as both oxidants and substrates, then as cross-coupling partners, to afford chiral polyfunctionalized amines. The strategy relies on an initial catalytic auto C(sp3)?H amination of the iodine(III) oxidant, which delivers an amine-derived iodine(I) product that is subsequently used in palladium-catalyzed cross-couplings to afford a variety of useful building blocks with high yields and excellent stereoselectivities. This study demonstrates the concept of self-amination of the hypervalent iodine reagents, which increases the value of the aryl moiety.
