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(Z)-3-(3-hydroxyphenyl)-2-(4-nitrophenyl)acrylonitrile is a complex organic compound characterized by its unique molecular structure. It features a conjugated triple bond (acrylonitrile) with two phenyl rings attached to it. One of the phenyl rings has a hydroxyl group at the 3rd position, while the other has a nitro group at the 4th position. (Z)-3-(3-hydroxyphenyl)-2-(4-nitrophenyl)acrylonitrile is known for its distinct electronic properties due to the presence of both electron-donating (hydroxyl) and electron-withdrawing (nitro) groups, which can influence its reactivity and potential applications in various chemical and pharmaceutical processes.

50632-38-7

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50632-38-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50632-38-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,3 and 2 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 50632-38:
(7*5)+(6*0)+(5*6)+(4*3)+(3*2)+(2*3)+(1*8)=97
97 % 10 = 7
So 50632-38-7 is a valid CAS Registry Number.

50632-38-7Downstream Products

50632-38-7Relevant academic research and scientific papers

Efficient and reusable amine-functionalized polyacrylonitrile fiber catalysts for Knoevenagel condensation in water

Li, Guowei,Xiao, Jia,Zhang, Wenqin

, p. 2234 - 2242 (2012)

A series of new fiber catalysts has been synthesized by aminating a commercially available polyacrylonitrile fiber with polyamines such as diethylenetriamine and triethylenetetramine. These fiber catalysts can efficiently catalyze the Knoevenagel condensation of benzaldehyde and ethyl cyanoacetate in water (yields: 95-98%). The triethylenetetramine aminated fiber catalyst was used to catalyze the condensations of a wide range of aromatic aldehydes and active methylene compounds and in each case, this catalyst performed well with yields higher than 93%. This fiber catalyst also exhibited excellent reusability (up to 21 times) and photostability.

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