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3,3-diphenyl-5-phenyl-3,3a,4,5,6,6a-hexahydropyrrolo[3,4-c]pyrazole is a complex organic compound with a unique molecular structure. It is characterized by a hexahydropyrrolo[3,4-c]pyrazole core, which is a fused ring system consisting of a pyrrole and a pyrazole. The molecule features three phenyl groups attached to the 3, 3, and 5 positions, respectively, providing it with a significant degree of steric hindrance and aromatic character. 3,3-diphenyl-5-phenyl-3,3a,4,5,6,6a-hexahydropyrrolo[3,4-c]pyrazole is of interest in the field of organic chemistry, potentially for its properties and reactivity, although specific applications or uses are not widely documented. The compound's structure suggests it may have unique electronic and steric properties that could be explored in various chemical contexts.

2997-61-7

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2997-61-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2997-61-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,9 and 7 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2997-61:
(6*2)+(5*9)+(4*9)+(3*7)+(2*6)+(1*1)=127
127 % 10 = 7
So 2997-61-7 is a valid CAS Registry Number.

2997-61-7Relevant academic research and scientific papers

Solid-state photochemistry of crystalline pyrazolines: Reliable generation and reactivity control of 1,3-biradicals and their potential for the green chemistry synthesis of substituted cyclopropanes

Shiraki, Saori,Vogelsberg, Cortnie S.,Garcia-Garibay, Miguel A.

, p. 1929 - 1937 (2013/01/16)

To expand on the limited number of examples that exist in the literature for the solid-state photodenitrogenation of azoalkanes, a series of crystalline 7-alkyl-2,3,7-triazabicyclo[3.3.0]oct-2-ene-6,8-diones with varying 4,4-substituents were prepared. Th

Synthesis and chemistry of pyrazolines derived from diphenyldiazomethane

Louhichi, Nesrine,Haouas, Amel,Hamadi, Naoufel Ben,Msaddek, Moncef

experimental part, p. 215 - 218 (2012/03/10)

The reaction of diphenyldiazomethane with N-substituted maleimides produces Δ 1-pyrazolines. The photolysis of Δ 1-pyrazolines leads to cyclopropanes. 2011 · Copyright by Walter de Gruyter.

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

Molchanov,Diev,Kostikov

, p. 259 - 263 (2007/10/03)

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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