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3,3-diphenyl-5-p-tolyl-3a,6a-dihydro-3H-pyrrolo[3,4-c]pyrazole-4,6-dione is a complex organic compound with a unique molecular structure. It is characterized by the presence of two phenyl groups attached to the 3rd carbon, a p-tolyl group (a tolyl group with a para-methyl substitution) at the 5th position, and a dihydro-pyrrolo[3,4-c]pyrazole-4,6-dione core. This core structure features a pyrrole ring fused to a pyrazole ring, with the dihydro prefix indicating the presence of two hydrogen atoms in a reduced form. The compound is further defined by the 4,6-dione functional group, which consists of two carbonyl groups (C=O) at the 4th and 6th positions. This molecule is of interest in the field of organic chemistry, potentially for its unique properties or as a building block in the synthesis of more complex molecules.

3120-01-2

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3120-01-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3120-01-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,2 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3120-01:
(6*3)+(5*1)+(4*2)+(3*0)+(2*0)+(1*1)=32
32 % 10 = 2
So 3120-01-2 is a valid CAS Registry Number.

3120-01-2Relevant academic research and scientific papers

Reactions of aliphatic diazo compounds: IV. Reaction of diphenyldiazomethane with substituted imides of maleic and itaconic acids

Molchanov,Diev,Kostikov

, p. 259 - 263 (2002)

Diphenyldiazomethane regioselectively adds to 2-R-substituted maleimides to yield 1-pyrazoline derivatives, 1-R-7-aryl-6,8-dioxo-4,4-diphenyl-2,3,7-triazabicyclo[3.3.0]oct-2-enes that on heating liberate nitrogen to afford substituted 3-azabicyclo[3.1.0]h

REACTIVITY OF SUBSTITUTED DIAZOMETHANES IN 1,3-DIPOLAR CYCLOADDITION TO N-ARYLMALEIMIDES AND ARYLETHENES

Samuilov, Ya. D.,Movchan, A. I.,Solov'eva, S. E.,Konovalov, A. I.

, p. 1985 - 1988 (2007/10/02)

The reactivity of phenyl- and diphenyldiazomethanes in 1,3-dipolar cycloaddition to N-arylmaleimides and also of diphenyldiazomethane in reaction with aryl ethenes was studied.It was shown that all the investigated reactions are of the "1,3-dipole-donor,

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