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Trimethylsilyl catechollactate tris(trimethylsilyl) ether is a complex organic compound with the chemical formula C24H45O7Si4. It is a derivative of catechol, a type of phenol, where the hydroxyl groups are protected by trimethylsilyl (TMS) groups. Trimethylsilyl catechollactate tris(trimethylsilyl) ether is often used in organic synthesis and as a protecting group for catechol, which is a key intermediate in the synthesis of various pharmaceuticals and natural products. The TMS groups can be removed under mild acidic conditions, making Trimethylsilyl catechollactate tris(trimethylsilyl) ether a valuable tool for chemists to control the reactivity of catechol during complex reactions.

68595-72-2

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68595-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68595-72-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,5,9 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 68595-72:
(7*6)+(6*8)+(5*5)+(4*9)+(3*5)+(2*7)+(1*2)=182
182 % 10 = 2
So 68595-72-2 is a valid CAS Registry Number.

68595-72-2Downstream Products

68595-72-2Relevant academic research and scientific papers

Conversion of dehydrodiferulic acids by human intestinal microbiota

Braune, Annett,Bunzel, Mirko,Yonekura, Reiko,Blaut, Michael

experimental part, p. 3356 - 3362 (2010/06/16)

Plant cell wall associated dehydrodiferulic acids (DFA) are abundant components of cereal insoluble dietary fibers ingested by humans. The ability of human intestinal microbiota to convert DFA was studied in vitro by incubating 8-O-4- and 5-5-coupled DFA with fecal suspensions. 8-O-4-DFA was completely degraded by the intestinal microbiota of the majority of donors, yielding homovanillic acid, 3-(3,4-dihydroxyphenyl)propionic acid, and 3,4-dihydroxyphenylacetic acid as the main metabolites. The transient formation of ferulic acid and presumably 3-(3-hydroxy-4-methoxyphenyl)pyruvic acid suggests an initial cleavage of the ether bond. In contrast to 8-O-4-DFA, the 5-5-coupled DFA was not cleaved into monomers by any of the fecal suspensions. Only the side chains were hydrogenated and the methoxy groups were demethylated. The cleavage of DFA by human intestinal microbiota, which depended on their coupling type, may affect both the bioavailability of DFA and the degradability of DFA-coupled fiber in the gut.

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