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1-(4-(hexan-2-yl)phenyl)ethan-1-one is an organic compound with the molecular formula C15H20O. It is a derivative of acetophenone, featuring a phenyl ring with a hexan-2-yl substituent at the para position and an ethan-1-one group attached to the carbon atom. This chemical is characterized by its unique structure, which contributes to its distinct chemical properties and potential applications in various fields, such as pharmaceuticals, fragrances, and chemical synthesis. The compound's structure and properties make it a versatile building block for the development of new molecules and compounds with specific functionalities.

7641-85-2

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7641-85-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7641-85-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,4 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7641-85:
(6*7)+(5*6)+(4*4)+(3*1)+(2*8)+(1*5)=112
112 % 10 = 2
So 7641-85-2 is a valid CAS Registry Number.

7641-85-2Downstream Products

7641-85-2Relevant academic research and scientific papers

Ni-catalyzed Reductive Deaminative Arylation at sp3 Carbon Centers

Martin-Montero, Raul,Yatham, Veera Reddy,Yin, Hongfei,Davies, Jacob,Martin, Ruben

, p. 2947 - 2951 (2019/04/30)

A Ni-catalyzed reductive deaminative arylation at unactivated sp3 carbon centers is described. This operationally simple and user-friendly protocol exhibits excellent chemoselectivity profile and broad substrate scope, thus complementing existing metal-catalyzed cross-coupling reactions to forge sp3 C-C linkages. These virtues have been assessed in the context of late-stage functionalization, hence providing a strategic advantage to reliably generate structure diversity with amine-containing drugs.

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