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3,4-di-O-allyl caffeic acid chloride is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

797041-01-1

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797041-01-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 797041-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,7,0,4 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 797041-01:
(8*7)+(7*9)+(6*7)+(5*0)+(4*4)+(3*1)+(2*0)+(1*1)=181
181 % 10 = 1
So 797041-01-1 is a valid CAS Registry Number.

797041-01-1Relevant academic research and scientific papers

First diastereoselective synthesis of methyl caffeoyl- and feruloyl-muco-quinates

Jaiswal, Rakesh,Dickman, Michael H.,Kuhnert, Nikolai

experimental part, p. 5266 - 5277 (2012/08/08)

We report on a diastereoselective synthesis of six derivatives of caffeoyl- and feruloyl-muco-quinic acids. All the muco-quinic acid derivatives were obtained in excellent yield in five steps starting from quinic acid, caffeic acid and ferulic acid. Allyl ether protection of trans-hydroxy cinnamic acids was here introduced to chlorogenic acids synthesis. We show that muco-quinic acid derivatives, which are formally diastereoisomers of chlorogenic acids, can be readily distinguished by their tandem mass spectra. The Royal Society of Chemistry 2012.

A non-enzymatic synthesis of (S)-(-)-rosmarinic acid and a study of a biomimetic route to (+)-rabdosiin

Bogucki, David E.,Charlton, James L.

, p. 1783 - 1794 (2007/10/03)

The synthesis of (S)-(-)-rosmarinic acid (30) in 9% overall yield is described. The synthesis was achieved by a convergent route in which 3-(3′,4′-dihydroxyphenyl)-(S)-lactic acid (23) and caffeic acid (25), both appropriately protected, were coupled to produce a pentaallyl precursor 29, which was then deprotected to give (S)-(-)-rosmarinic acid (30). A triallyl derivative 35 was similarly prepared and converted to (+)-rabdosiin (41) and its (1R,2S) isomer (42) via a biomimetic oxidative free radical coupling-cyclization followed by deallylation. The coupling-cyclization gave a ratio of rabdosiin diastereomers unlike that found in nature. A preliminary study showed that methyl (R)-mandelyl sinapate (15) could be dimerized diastereoselectively to give a 1,2-trans thomasidioate diester (16). The synthesis of (S)-(-)-rosmarinic aid (30) in 9% overall yield is described. The synthesis was achieved by a convergent route in which 3- (3',4'-dihydroxyphenyl)-(S)-lactic acid (23) and caffeic acid (25), both appropriately protected, were coupled to produce a pentaallyl precursor 29, which was then deprotected to give (S)-(-)-rosmarinic acid (30). A triallyl derivative 35 was similarly prepared and converted to (+)-rabdosiin (41) and its (1R,2S) isomer (42) via a biomimetic oxidative free radical coupling- cyclization followed by deallylation. The coupling-cyclization gave a ratio of rabdosiin diastereomers unlike that found in nature. A preliminary study showed that methyl (R)-mandelyl sinapate (15) could be dimerized diastereoselectively to give a 1,2-trans thomasidioate diester (16).

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