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1-Cyclopentyl-4-ethoxybenzene is an organic compound characterized by a benzene ring with a cyclopentyl group attached to the 1-position and an ethoxy group at the 4-position. This molecule, with the chemical formula C15H20O, features a combination of a cyclic alkane (cyclopentyl) and an ether (ethoxy) functional group, which contributes to its unique chemical properties. The cyclopentyl group provides a five-membered ring structure, while the ethoxy group introduces an oxygen atom bonded to an ethyl group, enhancing the molecule's reactivity and solubility. 1-cyclopentyl-4-ethoxybenzene is typically synthesized for use in the chemical and pharmaceutical industries, where it may serve as an intermediate in the production of various compounds or as a solvent. Its specific applications can vary, but the structural diversity it offers makes it a valuable component in the development of new chemical entities.

2206-49-7

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2206-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2206-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,0 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2206-49:
(6*2)+(5*2)+(4*0)+(3*6)+(2*4)+(1*9)=57
57 % 10 = 7
So 2206-49-7 is a valid CAS Registry Number.

2206-49-7Downstream Products

2206-49-7Relevant academic research and scientific papers

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Alkyl Bromides: Et3N as the Terminal Reductant

Duan, Zhengli,Li, Wu,Lei, Aiwen

, p. 4012 - 4015 (2016)

Reductive cross-coupling has emerged as a direct method for the construction of carbon-carbon bonds. Most cobalt-, nickel-, and palladium-catalyzed reductive cross-coupling reactions to date are limited to stoichiometric Mn(0) or Zn(0) as the reductant. One nickel-catalyzed cross-coupling paradigm using Et3N as the terminal reductant is reported. By using this photoredox catalysis and nickel catalysis approach, a direct Csp2-Csp3 reductive cross-coupling of aryl bromides with alkyl bromides is achieved under mild conditions without stoichiometric metal reductants.

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