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2-methyl-5-phenylpent-1-en-3-yl acetate is a chemical compound with the molecular formula C15H18O2. It is an organic ester derived from 2-methyl-5-phenylpent-1-en-3-ol and acetic acid. 2-methyl-5-phenylpent-1-en-3-yl acetate is characterized by a pentenyl chain with a methyl group at the 2nd carbon, a phenyl group at the 5th carbon, and an acetate group at the 3rd carbon. It is a colorless liquid with a fruity, floral odor and is used in the fragrance industry as a fixative and modifier in various perfume compositions. The compound is also known for its potential applications in the synthesis of pharmaceuticals and other organic compounds.

2283-24-1

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2283-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2283-24-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2283-24:
(6*2)+(5*2)+(4*8)+(3*3)+(2*2)+(1*4)=71
71 % 10 = 1
So 2283-24-1 is a valid CAS Registry Number.

2283-24-1Relevant academic research and scientific papers

Atmospheric Oxygen Mediated Radical Hydrothiolation of Alkenes

McCourt, Ruairí O.,Scanlan, Eoin M.

supporting information, p. 15804 - 15810 (2020/10/26)

A mild, metal-free, atmospheric oxygen-mediated radical hydrothiolation of alkenes (and alkyne) is reported. A variety of sulfur containing motifs including alkanethiols, thiophenols and thioacids undergo an atmospheric oxygen-mediated radical hydrothiolation reaction with a plethora of alkenes in good yield with excellent functional group compatibility, typically with short reaction times to furnish a range of functionalized products. Biomolecules proved tolerant to the conditions and the procedure is robust and easily executable requiring no specialized equipment. Concise mechanistic studies confirm the process proceeds through radical intermediates in a thiol-ene reaction manifold. The methodology offers an efficient “green” approach for thiol-ene mediated “click” ligation and a milder alternative to thermally initiated hydrothiolation processes.

Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2

Moragas, Toni,Cornella, Josep,Martin, Ruben

supporting information, p. 17702 - 17705 (2015/02/19)

A novel Ni-catalyzed regiodivergent reductive carboxylation of allyl esters with CO2 has been developed. This mild, user-friendly, and operationally simple method is characterized by an exquisite selectivity profile that is dictated by the ligand backbone.

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