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1-(4-(but-3-en-1-yl)phenyl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15451-36-2

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15451-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15451-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,5 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15451-36:
(7*1)+(6*5)+(5*4)+(4*5)+(3*1)+(2*3)+(1*6)=92
92 % 10 = 2
So 15451-36-2 is a valid CAS Registry Number.

15451-36-2Downstream Products

15451-36-2Relevant academic research and scientific papers

Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate

Hashizume, Daisuke,Hosoya, Takamitsu,Nakamura, Kei,Ohmiya, Hirohisa,Sato, Yukiya,Sumida, Yuto

supporting information, p. 9938 - 9943 (2020/06/27)

The generation of tertiary, secondary, and primary alkyl radicals has been achieved by the direct visible-light excitation of a boracene-based alkylborate. This system is based on the photophysical properties of the organoboron molecule. The protocol is applicable to decyanoalkylation, Giese addition, and nickel-catalyzed carbon-carbon bond formations such as alkyl-aryl cross-coupling or vicinal alkylarylation of alkenes, enabling the introduction of various C(sp3) fragments to organic molecules.

Ni-catalyzed Reductive Deaminative Arylation at sp3 Carbon Centers

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

supporting information, 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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