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(E)-1-deuterium-3-phenyl-2-butenal is a chemical compound with the molecular formula C10H9DO. It is an organic molecule that belongs to the class of aldehydes, characterized by the presence of a carbonyl group (C=O) at the end of a carbon chain. The compound features a deuterium atom (D), which is a stable isotope of hydrogen, attached to the first carbon atom. The phenyl group (C6H5) is attached to the third carbon atom, and the molecule has a trans (E) configuration, indicating that the phenyl group and the aldehyde group are on opposite sides of the double bond. (E)-1-deuterium-3-phenyl-2-butenal is used in various chemical reactions and as an intermediate in the synthesis of other organic compounds.

21866-71-7

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21866-71-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21866-71-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,6 and 6 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 21866-71:
(7*2)+(6*1)+(5*8)+(4*6)+(3*6)+(2*7)+(1*1)=117
117 % 10 = 7
So 21866-71-7 is a valid CAS Registry Number.

21866-71-7Relevant academic research and scientific papers

A versatile new catalyst for the enantioselective isomerization of allylic alcohols to aldehydes: Scope and mechanistic studies

Tanaka, Ken,Fu, Gregory C.

, p. 8177 - 8186 (2007/10/03)

A new planar-chiral bidentate phosphaferrocene ligand (2) has been synthesized and structurally characterized. The derived rhodium complex, [Rh(cod)(2)]BF4, serves as an effective catalyst for asymmetric isomerizations of allylic alcohols to aldehydes, furnishing improved yields, scope, and enantioselectivities relative to previously reported methods. The catalyst is air-stable and can be recovered at the end of the reaction. Mechanistic studies establish that the isomerization proceeds via an intramolecular 1,3-hydrogen migration and that the catalyst differentiates between the enantiotopic C1 hydrogens.

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