60463-12-9 Usage
Description
5-HYDROXY-2-NITROBENZYL ALCOHOL is an organic compound with the molecular formula C7H7NO4. It is characterized by the presence of a hydroxyl group at the 5th position and a nitro group at the 2nd position of the benzyl alcohol structure. 5-HYDROXY-2-NITROBENZYL ALCOHOL is known for its potential applications in various chemical and pharmaceutical processes due to its unique functional groups.
Uses
Used in Chemical Synthesis:
5-HYDROXY-2-NITROBENZYL ALCOHOL is used as a key intermediate in the synthesis of various organic compounds. Its hydroxyl and nitro groups can be further modified or reacted with other molecules to produce a wide range of products.
Used in Pharmaceutical Applications:
5-HYDROXY-2-NITROBENZYL ALCOHOL is used as a starting material for the development of new pharmaceutical compounds. Its unique structure and functional groups can be exploited to design and synthesize novel drugs with potential therapeutic applications.
Used in Polymer Science:
5-HYDROXY-2-NITROBENZYL ALCOHOL is used as a difunctional photo-responsive initiator in the synthesis of thermo-responsive and photo-cleavable amphiphilic block copolymers. These copolymers contain photodegradable linkers as junction points between hydrophilic and hydrophobic chains, which can be utilized in various applications such as drug delivery systems, self-assembling materials, and stimuli-responsive materials.
Used in the Synthesis of 5-(2′-(DIMETHYLAMINO)ETHOXY)-2-NITROBENZYL ALCOHOL:
5-HYDROXY-2-NITROBENZYL ALCOHOL is used as a precursor in the synthesis of 5-(2′-(dimethylamino)ethoxy)-2-nitrobenzyl alcohol. This derivative can be employed in various applications, such as photochemical reactions and the development of new materials with unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 60463-12-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,4,6 and 3 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60463-12:
(7*6)+(6*0)+(5*4)+(4*6)+(3*3)+(2*1)+(1*2)=99
99 % 10 = 9
So 60463-12-9 is a valid CAS Registry Number.
InChI:InChI=1/C7H7NO4/c9-4-5-3-6(10)1-2-7(5)8(11)12/h1-3,9-10H,4H2
60463-12-9Relevant articles and documents
Synthesis of photocleavable poly(methyl methacrylate-block- d -lactide) via atom-transfer radical polymerization and ring-opening polymerization
Li, Hong,Rathi, Sahas,Sterner, Elizabeth S.,Zhao, Hui,Ling Hsu, Shaw,Theato, Patrick,Zhang, Yongming,Bryan Coughlin
, p. 4309 - 4316 (2013)
The synthesis and characterization of a photocleavable block copolymer containing an ortho-nitrobenzyl (ONB) linker between poly(methyl methacrylate) and poly(d-lactide) blocks is presented here. The block copolymers were synthesized via atom transfer rad
Preparation and application of a dual light-responsive triblock terpolymer
Rabnawaz, Muhammad,Liu, Guojun
, p. 5586 - 5595 (2012)
Reported are the preparation and application of a triblock terpolymer poly(ethylene oxide)-ONB-poly[2-(perfluorooctyl)ethyl methacrylate]-block- poly(2-cinnamoyloxyethyl methacrylate) (PEO-ONB-PFOEMA-b-PCEMA). Here PEO is water-soluble, PCEMA is photo-cro
Synthesis of Photo, Oxidative, and Reductive Triple-Stimuli-Responsive Block Copolymer Micelles as Nanocarriers for Controlled Release
Guo, Qiong,Liu, Jiangtao,Yang, Hong,Lei, Zhongli
, p. 363 - 373 (2022/01/04)
With the rapid development of nanotechnology, stimuli-responsive nanomaterials have provided an alternative for designing controllable drug delivery systems due to their spatiotemporally controllable properties. The environment of the human body is comple
Light-Responsive, Shape-Switchable Block Copolymer Particles
Lee, Junhyuk,Ku, Kang Hee,Kim, Jinwoo,Lee, Young Jun,Jang, Se Gyu,Kim, Bumjoon J.
supporting information, p. 15348 - 15355 (2019/10/02)
A robust strategy is developed for preparing light-responsive block copolymer (BCP) particles in which shape and color can be actively controlled with high spatial and temporal resolution. The key to achieving light-responsive shape transitions of BCP par