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Isopropyl 4-vinylbenzoate, also known as 4-isopropylstylol, is an organic compound with the chemical formula C12H14O2. It is a colorless to pale yellow liquid that is insoluble in water but soluble in organic solvents. This ester is derived from the combination of isopropyl alcohol and 4-vinylbenzoic acid, and it is commonly used as a fragrance ingredient in various personal care products, such as perfumes and deodorants, due to its pleasant, floral scent. Additionally, isopropyl 4-vinylbenzoate has applications in the pharmaceutical industry as a chemical intermediate and in the synthesis of other organic compounds. It is important to note that, like many chemicals, it should be handled with care due to potential health and environmental concerns.

2715-40-4

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2715-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2715-40-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,1 and 5 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 2715-40:
(6*2)+(5*7)+(4*1)+(3*5)+(2*4)+(1*0)=74
74 % 10 = 4
So 2715-40-4 is a valid CAS Registry Number.

2715-40-4Downstream Products

2715-40-4Relevant academic research and scientific papers

Rhodium-Catalyzed Hydrocarboxylation of Olefins with Carbon Dioxide

Kawashima, Shingo,Aikawa, Kohsuke,Mikami, Koichi

, p. 3166 - 3170 (2016)

The catalytic hydrocarboxylation of styrenes derivatives and α,β-unsaturated carbonyl compounds with CO2(101.3 kPa) in the presence of an air-stable rhodium catalyst was explored. The combination of [RhCl(cod)]2(cod = cyclooctadiene) as a catalyst and diethylzinc as a hydride source allowed for effective hydrocarboxylation and provided the corresponding α-aryl carboxylic acids in moderate to excellent yields. In this catalytic process with carbon dioxide, intervention of the RhI–H species, which could be generated from the RhIcatalyst and diethylzinc, was clarified. Significantly, the catalytic asymmetric hydrocarboxylation of α,β-unsaturated esters with carbon dioxide was also performed by employing a cationic rhodium complex possessing (S)-(–)-4,4′-bi-1,3-benzodioxole-5,5′-diylbis(diphenylphosphine) [(S)-SEGPHOS] as a chiral diphosphine ligand. A plausible model for asymmetric induction was proposed by determination of the absolute configuration of the product.

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