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α-Deuterated benzaldehyde dimethyl acetal is a chemical compound derived from benzaldehyde, where one of the hydrogen atoms on the alpha carbon (the carbon atom directly attached to the carbonyl group) is replaced with a deuterium atom. This deuterium substitution can affect the compound's chemical reactivity and physical properties, such as its boiling point and solubility. The dimethyl acetal functional group, formed by the reaction of benzaldehyde with two molecules of methanol, provides the compound with a distinct odor and reactivity profile. α-deuterated benzaldehyde dimethyl acetal is used in various applications, including as a synthetic intermediate in the preparation of deuterated organic compounds and in the study of reaction mechanisms involving deuterium-labeled molecules.

82736-93-4

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82736-93-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82736-93-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,3 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82736-93:
(7*8)+(6*2)+(5*7)+(4*3)+(3*6)+(2*9)+(1*3)=154
154 % 10 = 4
So 82736-93-4 is a valid CAS Registry Number.

82736-93-4Relevant academic research and scientific papers

Reductive openings of benzylidene acetals revisited: A mechanistic scheme for regio- and stereoselectivity

Johnsson, Richard,Ohlin, Markus,Ellervik, Ulf

supporting information; experimental part, p. 8003 - 8011 (2011/03/18)

Despite the importance of regioselective reductive openings of cyclic acetals, mechanistic details are scarce. In this study 4,6-O-benzylidene acetals were used as model compounds for deciphering the mechanism of regioselective openings using a variety of

HYPERVALENT IODINE IN ORGANIC SYNTHESIS. ACETAL FORMATION UNDER BASIC CONDITIONS AND CARBON DEUTERIATION OF THE ALDEHYDO GROUP

Moriarty, Robert M.,Hu, Henry

, p. 1537 - 1540 (2007/10/02)

Aldazines upon treatment with phenyliodosyl diacetate in CH3OH or CH3OD and NaOCH3 are converted smoothly into two equivalents of the corresponding aldehyde dimethylacetal with deuterium incorporation at the aldehydic carbon atom in the case of CH3OD.

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