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(E)-<(E)-benzylideneacetone> oxime O-methyl ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33652-67-4

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33652-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33652-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,5 and 2 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 33652-67:
(7*3)+(6*3)+(5*6)+(4*5)+(3*2)+(2*6)+(1*7)=114
114 % 10 = 4
So 33652-67-4 is a valid CAS Registry Number.

33652-67-4Relevant academic research and scientific papers

Reaction of dibenzylphosphine oxide with α,β-unsaturated O-methyloximes

Kolesnik,Tkachev

, p. 624 - 629 (2007/10/03)

The reaction of dibenzylphosphine oxide with O-methyloximes of some α,β-unsaturated ketones results in the phosphorylation at the β-carbon atom to form methoxyiminophosphine oxides, whereas the reaction of dibenzylphosphine oxide with O-methyloximes of α,β-unsaturated aldehydes affords aminodihydrophosphole oxides.

Photochemistry of the Carbon-Nitrogen Double Bond. Part 1. Carbon-Nitrogen vs. Carbon-Carbon Double Bond Isomerisation in the Photochemistry of α,β-Unsaturated Oxime Ethers: The Benzylideneacetone Oxime O-Methyl Ether System

Pratt, Albert C.,Abdul-Majid, Qais

, p. 1691 - 1694 (2007/10/02)

The syntheses of the four benzylideneacetone oxime O-methyl ether isomers (2)-(5) are described.Direct or sensitised irradiation of the E,E-isomer (2) or Z,E-isomer (3) leads to equilibration of all four isomers by a combination of rapid carbon-nitrogen double bond isomerisation and slower carbon-carbon double bond isomerisation.A previous investigation of the photochemistry of the E,E-isomer (2) had reported only carbon-carbon double bond isomerisation.

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