3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.SDS of cas: 60463-12-9
Synthesis of photocleavable poly(methyl methacrylate-block-D-lactide) via atom-transfer radical polymerization and ring-opening polymerization was written by Li, Hong;Rathi, Sahas;Sterner, Elizabeth S.;Zhao, Hui;Hsu, Shaw Ling;Theato, Patrick;Zhang, Yongming;Coughlin, E. Bryan. And the article was included in Journal of Polymer Science, Part A: Polymer Chemistry in 2013.SDS of cas: 60463-12-9 This article mentions the following:
The synthesis and characterization of a photocleavable block copolymer containing an ortho-nitrobenzyl (ONB) linker between poly(Me methacrylate) and poly(D-lactide) blocks is presented here. The block copolymers were synthesized via atom transfer radical polymerization (ATRP) of MMA followed by ring-opening polymerization (ROP) of D-Lactide and ROP of D-lactide followed by ATRP of MMA from a difunctional photoresponsive ONB initiator, resp. The challenges and limitations during synthesis of the photocleavable block copolymers using the difunctional photoresponsive ONB initiator are discussed. The photocleavage of the copolymers occurs under mild conditions by simple irradiation with 302 nm wavelength UV light (Relative intensity at 7.6 cm: 1500 μW/cm2) for several hours. In the experiment, the researchers used many compounds, for example, 3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9SDS of cas: 60463-12-9).
3-(Hydroxymethyl)-4-nitrophenol (cas: 60463-12-9) belongs to alcohols. Under appropriate conditions, inorganic acids also react with alcohols to form esters. To form these esters, a wide variety of specialized reagents and conditions can be used. Under carefully controlled conditions, simple alcohols can undergo intermolecular dehydration to give ethers. This reaction is effective only with methanol, ethanol, and other simple primary alcohols.SDS of cas: 60463-12-9
Referemce:
Alcohol – Wikipedia,
Alcohols – Chemistry LibreTexts