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Benzaldehyde N-methyl-N-benzoylhydrazone is a chemical compound with the molecular formula C15H15N2O. It is a derivative of benzaldehyde, where the aldehyde group has been converted into a hydrazone by reacting with N-methylbenzoylhydrazine. benzaldehyde N-methyl-N-benzoylhydrazone is an off-white to pale yellow crystalline solid and is soluble in common organic solvents such as ethanol, acetone, and dichloromethane. It is used as an analytical reagent for the detection and determination of aldehydes and ketones due to its ability to form colored complexes with these compounds. Additionally, benzaldehyde N-methyl-N-benzoylhydrazone has potential applications in the synthesis of various organic compounds and pharmaceuticals.

1924-86-3

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1924-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1924-86-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,2 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1924-86:
(6*1)+(5*9)+(4*2)+(3*4)+(2*8)+(1*6)=93
93 % 10 = 3
So 1924-86-3 is a valid CAS Registry Number.

1924-86-3Relevant academic research and scientific papers

PHOSPHORUS ANALOGUES OF AMINO ACIDS AND PEPTIDES XII. REACTION OF SODIUM DIETHYL PHOSPHITE WITH AROMATIC ALDAZINES AND HYDRAZONES

Topolski, M.,Rachon, J.

, p. 97 - 110 (2007/10/02)

The mechanism of the reaction of sodium diethyl phosphite with aromatic aldazines has been investigated.The initially formed monoaddition product (4) reacts with the excess of phosphorus reagent prior to the conceivable addition of diethyl phosphite to the C=N double bond.Cleavage of the N-N single bond is initiated by Single Electron Transfer from phosphite anion to the conjugated N=CH-Ph bond system.The scope of the reaction can be extended to other aromatic hydrazones.There is strong evidence to support the operation of a non-chain SET mechanism.

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