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α-Methoxyphenylacetaldehyde ethylene acetal is a chemical compound with the molecular formula C11H14O3. It is an organic compound derived from α-methoxyphenylacetaldehyde, where an ethylene acetal group is attached to the aldehyde functional group. α-methoxyphenylacetaldehyde ethylene acetal is characterized by its aromatic ring with a methoxy group (-OCH3) and an ethylene acetal (-CH2OCH2-) moiety, which contributes to its unique chemical properties and reactivity. It is used in the synthesis of various organic compounds and can be found in the fragrance and flavor industry due to its pleasant odor. The ethylene acetal group provides stability to the molecule and can participate in various chemical reactions, making it a valuable intermediate in organic synthesis.

72700-10-8

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72700-10-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72700-10-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,7,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 72700-10:
(7*7)+(6*2)+(5*7)+(4*0)+(3*0)+(2*1)+(1*0)=98
98 % 10 = 8
So 72700-10-8 is a valid CAS Registry Number.

72700-10-8Downstream Products

72700-10-8Relevant academic research and scientific papers

SELENIUM CATALYZED CONVERSION OF VINYL HALIDES INTO α-ALKOXY ACETALS

Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco,Chianelli, Donatella,Bartoli, Donatella

, p. 2273 - 2282 (2007/10/02)

The reaction of vinyl halides with phenylselenenyl chloride in alcohols affords α-alkoxy acetals and diphenyl diselenide which can be oxidized to PhSe cations by nitrate or persulfate anions.The reaction can be carried out with catalytic amounts of PhSeCl or PhSeSePh.The reaction proceeds through the formation of the methoxyselenenylation product which then suffers solvolysis.Under controlled conditions, the 1-phenyl-1-methoxy-2-bromo-2-phenylselenenyl ethane was isolated from the reaction of β-bromostyrene and PhSeCl in methanol.Several deselenenylation reactions of this α-halogenoselenide are reported.

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