Synthesis of N-protected serine ethers as precursors of new photoactivatable amino acids cleavable by hydrogenolysis was written by Dugave, Christophe;Kessler, Pascal;Colas, Christophe;Hirth, Christian. And the article was included in Tetrahedron Letters in 1994.Name: 3-(Hydroxymethyl)-4-nitrophenol This article mentions the following:
Protected serine amino(hydroxy)benzyl ethers I (Boc = Me3CO2C, Fmoc = 9-fluorenylmethoxycarbonyl, MEM = 2-methoxyethoxymethyl) were synthesized. Spectral characteristics of the corresponding photoactivatable 4-diazocyclohexa-2,5-dienones II were determined In the experiment, the researchers used many compounds, for example, 3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9Name: 3-(Hydroxymethyl)-4-nitrophenol).
3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9) belongs to alcohols. Alcohols are weak acids. The most acidic simple alcohols (methanol and ethanol) are about as acidic as water, and most other alcohols are somewhat less acidic. Grignard and organolithium reagents are powerful tools for organic synthesis, and the most common products of their reactions are alcohols.Name: 3-(Hydroxymethyl)-4-nitrophenol
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts