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(Ε)-N-(2-nitrobenzylidene)aniline is an organic compound with the chemical formula C13H10N2O2. It is a yellow crystalline solid that is formed by the condensation of 2-nitrobenzaldehyde with aniline. (Ε)-N-(2-nitrobenzylidene)aniline is characterized by its nitro group (-NO2) attached to the benzene ring and an aniline group (-NHPh) connected to the double bond. It is often used as a photochromic compound due to its ability to undergo reversible photoisomerization between the closed (spirocyclic) and open (zwitterionic) forms upon exposure to light, which results in a change in color. This property makes it a potential candidate for applications in optical data storage, molecular switches, and other areas where reversible color changes are desired.

1624-50-6

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1624-50-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1624-50-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,6,2 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1624-50:
(6*1)+(5*6)+(4*2)+(3*4)+(2*5)+(1*0)=66
66 % 10 = 6
So 1624-50-6 is a valid CAS Registry Number.

1624-50-6Relevant academic research and scientific papers

Acceptorless dehydrogenative construction of CN and CC bonds through catalytic aza-Wittig and Wittig reactions in the presence of an air-stable ruthenium pincer complex

Biswas, Nandita,Das, Kalicharan,Sardar, Bitan,Srimani, DIpankar

, p. 6501 - 6512 (2019)

The construction of CN bonds was achieved by the dehydrogenative coupling of alcohol and azide via aza-Wittig type reaction. The reaction is catalyzed by an acridine-derived ruthenium pincer complex and does not use any oxidant. The present protocol offers a wide substrate scope, including aliphatic, aryl or heteroaryl alcohol/azides. This expeditious protocol was successfully applied to construct a CC bond directly from alcohol via dehydrogenative Wittig reaction. Furthermore, the synthesis of structurally important pyrrolo[1,4]benzodiazepine derivatives was also achieved by this methodology.

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