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1-(4-Nitro-phenyl)-7a-pyrrolidin-1-yl-3a,4,5,6,7,7a-hexahydro-1H-benzotriazole is a complex organic compound with the molecular formula C16H20N4O2. It is a derivative of benzotriazole, featuring a pyrrolidine ring and a nitrophenyl group. 1-(4-Nitro-phenyl)-7a-pyrrolidin-1-yl-3a,4,5,6,7,7a-hexahydro-1H-benzotriazole is characterized by its hexahydro structure, which contributes to its stability and reactivity. It is often used in chemical research and synthesis due to its unique properties and potential applications in the development of new materials and pharmaceuticals. The presence of the nitro group and the pyrrolidine ring make it a versatile building block for further chemical modifications and reactions.

2082-97-5

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2082-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2082-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,8 and 2 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2082-97:
(6*2)+(5*0)+(4*8)+(3*2)+(2*9)+(1*7)=75
75 % 10 = 5
So 2082-97-5 is a valid CAS Registry Number.

2082-97-5Downstream Products

2082-97-5Relevant academic research and scientific papers

Thermochemical and kinetic investigation of 1,3-dipolar cycloaddition reactions involving aryl azides and nitrones

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

, p. 1618 - 1622 (2007/10/02)

The 1,3-dipolar cycloaddition reactions of aryl azides with pyrrolidinocyclohexene and endo-dicyclopentadiene and also of C-benzoyl-N-phenyl nitrone with substituted norbornenes were investigated by a thermochemical method.On the basis of the obtained data a comparison was made of the localization energies of the aryl azides and nitrones.In the reactions of C-benzoyl-N-phenyl nitrone with substituted norbornenes the opposite effects of the donor-acceptor interactions and the localization effects on the reactivity lead to loss of the sensitivity of the condensations to change in the electronic character of the substituents in the dipolarophile.

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