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α-Methyl-2-hydroxy-5-nitrocinnamaldehyde is an organic compound characterized by its molecular formula C10H9NO4. It features a cinnamaldehyde backbone, which is a type of aldehyde derived from cinnamic acid, with a methyl group attached to the alpha carbon, a hydroxyl group at the 2nd carbon, and a nitro group at the 5th carbon. α-methyl-2-hydroxy-5-nitrocinnamaldehyde is known for its potential applications in the synthesis of various pharmaceuticals and chemical intermediates due to its unique functional groups. The presence of the nitro group endows it with reactivity that can be exploited in reduction reactions, while the hydroxyl group allows for further functionalization. Its chemical properties make it a valuable building block in organic synthesis, particularly in the preparation of complex molecules with potential biological activity.

82380-83-4

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82380-83-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82380-83-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,8 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 82380-83:
(7*8)+(6*2)+(5*3)+(4*8)+(3*0)+(2*8)+(1*3)=134
134 % 10 = 4
So 82380-83-4 is a valid CAS Registry Number.

82380-83-4Downstream Products

82380-83-4Relevant academic research and scientific papers

REACTION OF FISCHER'S BASE WITH o-HYDROXYCINNAMALDEHYDES

Chunaev, Yu. M.,Przhiyalgovskaya, N. M.,Gal'bershtam, M. A.,Kurkovskaya, L. N.

, p. 265 - 268 (1982)

On the basis of a study of the PMR spectra and alternative synthesis it was established that the "dicondensed" products of the reaction of Fischer's base with o-hydroxycinnamaldehydes are not oxocine derivatives, as was previously assumed, but rather are

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