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4-Nitrophenylacetaldehyde 2,4-dinitrophenylhydrazone is a chemical compound with the molecular formula C14H10N4O5. It is formed by the reaction of 4-nitrophenylacetaldehyde with 2,4-dinitrophenylhydrazine, resulting in the formation of a hydrazone derivative. This yellow crystalline solid is an important intermediate in the synthesis of various organic compounds and has potential applications in the pharmaceutical and chemical industries. The compound is characterized by its distinct chemical structure, which includes a nitro group attached to a phenyl ring, an acetaldehyde moiety, and a 2,4-dinitrophenylhydrazone group. Due to its complex structure and reactivity, it is essential to handle 4-nitrophenylacetaldehyde 2,4-dinitrophenylhydrazone with care, following proper safety protocols and guidelines.

3756-36-3

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3756-36-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3756-36-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,5 and 6 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3756-36:
(6*3)+(5*7)+(4*5)+(3*6)+(2*3)+(1*6)=103
103 % 10 = 3
So 3756-36-3 is a valid CAS Registry Number.

3756-36-3Downstream Products

3756-36-3Relevant academic research and scientific papers

Efficient and highly aldehyde selective wacker oxidation

Teo, Peili,Wickens, Zachary K.,Dong, Guangbin,Grubbs, Robert H.

supporting information; experimental part, p. 3237 - 3239 (2012/08/27)

A method for efficient and aldehyde-selective Wacker oxidation of aryl-substituted olefins using PdCl2(MeCN)2, 1,4-benzoquinone, and t-BuOH in air is described. Up to a 96% yield of aldehyde can be obtained, and up to 99% selectivity can be achieved with styrene-related substrates.

Diazo reactions with unsaturated compounds: V.1 reaction of phenyl vinyl ether with arenediazonium chlorides

Naidan

, p. 1600 - 1602 (2007/10/03)

Phenyl vinyl ether reacts with arenediazonium chlorides in aqueous acetone at pH 3-4 in the presence of a catalytic amount of copper(II) chloride to give arylacetaldehydes and small amounts 1-aryl-2-phenoxyethenes. No reaction occurs between the same reactants in the presence of sulfur(IV) oxide. 2000 MAIK "Nauka/Interperiodica".

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