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1,1'-(5-{[(4-methoxyphenyl)amino]methyl}-Δ2-pyrazolin-3,5-diyl)bis(ethan-1-one) is a complex organic compound with the molecular formula C21H21N3O4. It features a pyrazoline core, which is a heterocyclic ring system consisting of two nitrogen atoms and one carbon-carbon double bond. The compound has two ethanone (acetone) groups attached to the pyrazoline core, and a 4-methoxyphenyl group connected to the pyrazoline through an aminomethyl linker. This structure contributes to its potential applications in various chemical and pharmaceutical fields, such as the synthesis of dyes, pigments, and pharmaceutical intermediates. The presence of the methoxy group and the amino group on the phenyl ring may also influence the compound's reactivity and physical properties, making it a subject of interest for further research and development.

4916-10-3

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4916-10-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4916-10-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 6 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 4916-10:
(6*4)+(5*9)+(4*1)+(3*6)+(2*1)+(1*0)=93
93 % 10 = 3
So 4916-10-3 is a valid CAS Registry Number.

4916-10-3Downstream Products

4916-10-3Relevant academic research and scientific papers

Cycloaddition Reactions of Azides and Electron-Deficient Alkenes in Deep Eutectic Solvents: Pyrazolines, Aziridines and Other Surprises

Casarrubios, Luis,Díez-González, Silvia,Lachhani, Kushal,Pimpasri, Chaleena,Rzepa, Henry S.,Sebest, Filip,White, Andrew J. P.

, (2020)

The reaction of organic azides and electron-deficient alkenes was investigated in a deep eutectic solvents. A series of highly substituted 2-pyrazolines was successfully isolated and their formation rationalised by DFT calculations. The critical effect of substitution was also explored; even relatively small changes in the cycloaddition partners led to completely different reaction outcomes and triazolines, triazoles or enaminones can be formed as major products depending on the alkene employed. (Figure presented.).

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