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Vinyl 4-chlorocinnamate, also known as 4-chloro-3-phenylprop-2-enoic acid, is an organic compound with the chemical formula C10H9ClO2. It is a colorless to pale yellow liquid with a molecular weight of 198.63 g/mol. vinyl 4-chlorocinnamate is characterized by the presence of a vinyl group (C=C) and a 4-chlorocinnamate group, which consists of a chlorine atom attached to a cinnamate moiety. Vinyl 4-chlorocinnamate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Due to its reactive nature, it is essential to handle vinyl 4-chlorocinnamate with care, following proper safety protocols to minimize potential health and environmental risks.

10604-65-6

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10604-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10604-65-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,6,0 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10604-65:
(7*1)+(6*0)+(5*6)+(4*0)+(3*4)+(2*6)+(1*5)=66
66 % 10 = 6
So 10604-65-6 is a valid CAS Registry Number.

10604-65-6Downstream Products

10604-65-6Relevant academic research and scientific papers

Dual Activity of Grubbs-Type Catalyst in the Transvinylation of Carboxylic Acids and Ring-Closing Metathesis Reactions

Brodzka, Anna,Koszelewski, Dominik,Ostaszewski, Ryszard,Brodzka, Anna,Ostaszewski, Ryszard

, p. 15305 - 15313 (2020)

The development of a multifunctional catalyst, which mimics the promiscuity of enzymes, that would catalyze more than one chemical transformation in a single reaction vessel is one of the key points of modern sustainable chemistry. The results of our experiments indicated that Grubbs-type catalysts possess such multitask activity, catalyzing the transvinylation reaction of carboxylic acids without losing their original metathetic activity. This new activity of Grubbs catalysts was evidenced on several examples. It allows us to design a transvinylation/ring-closing metathesis (RCM) cascade reaction leading to the formation of endocyclic enol lactones from unsaturated carboxylic acids in an one-pot procedure. This unique ability of Grubbs catalyst to catalyze multiple mechanically distinct cascade reactions in a chemoselective way offers the new possibility for the synthesis of complex compounds from simple, easily accessible substrates.

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