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1-(4-(heptan-2-yl)phenyl)ethan-1-one is an organic compound with the molecular formula C16H24O. It is a derivative of acetophenone, featuring a heptyl group attached to the phenyl ring at the para position. This ketone is characterized by its unique structure, where a seven-carbon alkyl chain (heptan-2-yl) is connected to the phenyl ring, and the carbonyl group is attached to the ethyl group. This chemical is primarily used as a synthetic intermediate in the production of various pharmaceuticals, fragrances, and other organic compounds. Its properties include a low solubility in water and high solubility in organic solvents, as well as a relatively low melting and boiling point. The compound is also known for its potential reactivity with nucleophiles and electrophiles, making it a versatile building block in organic synthesis.

7641-86-3

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7641-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7641-86-3 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 6 respectively.
Calculate Digit Verification of CAS Registry Number 7641-86:
(6*7)+(5*6)+(4*4)+(3*1)+(2*8)+(1*6)=113
113 % 10 = 3
So 7641-86-3 is a valid CAS Registry Number.

7641-86-3Upstream product

7641-86-3Downstream Products

7641-86-3Relevant 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)

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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