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α-Methyl-hydrozimtsaeure-isopropylester, also known as α-Methyl-hydrocinnamic acid isopropyl ester, is an organic compound with the chemical formula C12H16O2. It is a derivative of hydrocinnamic acid, featuring an α-methyl group attached to the hydrocinnamic acid structure. This ester is formed by the reaction of α-methyl-hydrocinnamic acid with isopropanol in the presence of an acid catalyst. It is a colorless to pale yellow liquid with a fruity, balsamic odor and is used as a fragrance ingredient in various applications, including perfumes and cosmetics. The compound is also known for its potential use in the synthesis of pharmaceuticals and agrochemicals.

75906-61-5

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75906-61-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 75906-61-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,9,0 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 75906-61:
(7*7)+(6*5)+(5*9)+(4*0)+(3*6)+(2*6)+(1*1)=155
155 % 10 = 5
So 75906-61-5 is a valid CAS Registry Number.

75906-61-5Downstream Products

75906-61-5Relevant academic research and scientific papers

Highly enantioselective iridium-catalyzed hydrogenation of α,β-unsaturated esters

Li, Jia-Qi,Quan, Xu,Andersson, Pher G.

supporting information, p. 10609 - 10616 (2012/11/07)

α,β-Unsaturated esters have been employed as substrates in iridium-catalyzed asymmetric hydrogenation. Full conversions and good to excellent enantioselectivities (up to 99 % ee) were obtained for a broad range of substrates with both aromatic- and aliphatic substituents on the prochiral carbon. The hydrogenated products are highly useful as building blocks in the synthesis of a variety of natural products and pharmaceuticals. Asymmetric hydrogenation: A variety of α,β-unsaturated esters were hydrogenated with high enantioselectivities (see scheme). The hydrogenated products have been used in synthetic transformations as well as in formal total syntheses. Copyright

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