28171-92-8 Usage
Description
(1-Naphthyl)methyl Methacrylate, also known as NMM, is a synthetic monomer derived from methacrylic acid and 1-naphthol. It possesses a unique molecular structure with a naphthalene ring and a methacrylate group, which endows it with specific chemical and physical properties. NMM is known for its high reactivity and compatibility with various polymerization processes, making it a versatile building block for the development of advanced polymer materials.
Uses
Used in Polymer Science:
(1-Naphthyl)methyl Methacrylate is used as a monomer for the synthesis of copolymers with tailored properties. The incorporation of NMM into the polymer backbone enhances the overall performance of the material, such as its mechanical strength, thermal stability, and chemical resistance.
Used in Fluorescent Probes:
(1-Naphthyl)methyl Methacrylate is used as a fluorescent probe for studying the interdiffusion of polymer latex. The naphthalene moiety in NMM provides a strong fluorescence signal, which can be utilized to monitor the diffusion process and gain insights into the interactions between different polymer species.
Used in Analytical Chemistry:
(1-Naphthyl)methyl Methacrylate can be employed as a derivatization agent for the analysis of various organic compounds. The reactive methacrylate group can be used to form covalent bonds with target molecules, facilitating their detection and quantification using fluorescence-based techniques.
Used in Pharmaceutical Industry:
(1-Naphthyl)methyl Methacrylate may find applications in the development of drug delivery systems, such as nanoparticles or hydrogels, for the controlled release of therapeutic agents. The unique properties of NMM can be exploited to design advanced drug carriers with enhanced stability, biocompatibility, and targeting capabilities.
Used in Material Science:
(1-Naphthyl)methyl Methacrylate can be utilized in the fabrication of advanced materials with specific optical, electronic, or mechanical properties. The naphthalene ring in NMM can contribute to the light absorption and emission characteristics of the material, making it suitable for applications in optoelectronics, sensors, and photonics.
Check Digit Verification of cas no
The CAS Registry Mumber 28171-92-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,7 and 1 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28171-92:
(7*2)+(6*8)+(5*1)+(4*7)+(3*1)+(2*9)+(1*2)=118
118 % 10 = 8
So 28171-92-8 is a valid CAS Registry Number.
28171-92-8Relevant articles and documents
Copper-catalyzed intermolecular chloroazidation of α,β-unsaturated amides
Chen, Long,Xing, Haotian,Zhang, Huaibin,Jiang, Zhong-Xing,Yang, Zhigang
, p. 7463 - 7467 (2016/08/16)
A highly practical copper-catalyzed intermolecular chloroazidation of α,β-unsaturated amides has been described, giving a series of azidochlorides in good-to-excellent yields. The stable azidoiodine(iii) reagent and SOCl2 were used as azide and chlorine sources, respectively. The synthetic applications of this protocol were also explored by a variety of synthetically useful transformations.
