2973-15-1 Usage
Uses
Used in Organic Synthesis:
(2-Nitrophenyl)maleimide is used as a key intermediate in organic synthesis for its ability to participate in Diels-Alder reactions, facilitating the creation of complex cyclic structures that are otherwise challenging to synthesize.
Used in Pharmaceutical Synthesis:
(2-Nitrophenyl)maleimide is utilized as a building block in the synthesis of biologically active molecules and pharmaceuticals, capitalizing on its strong electrophilic nature to form new compounds with potential therapeutic applications.
Used in Materials Science:
(2-Nitrophenyl)maleimide is employed in the development of optoelectronic devices and materials with specific optical properties, leveraging its chemical structure to engineer materials with tailored characteristics for various applications in the optoelectronic industry.
Used in Research:
(2-Nitrophenyl)maleimide serves as a valuable tool in academic and industrial research settings, where its unique reactivity and properties are explored for new applications and to advance understanding in the fields of chemistry and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 2973-15-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 3 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2973-15:
(6*2)+(5*9)+(4*7)+(3*3)+(2*1)+(1*5)=101
101 % 10 = 1
So 2973-15-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H6N2O4/c13-9-5-6-10(14)11(9)7-3-1-2-4-8(7)12(15)16/h1-6H
2973-15-1Relevant academic research and scientific papers
Regioselective ortho-nitration of N-phenyl carboxamides and primary anilines using bismuth nitrate/acetic anhydride
Lu, Yang,Li, Yaming,Zhang, Rong,Jin, Kun,Duan, Chunying
supporting information, p. 9422 - 9427 (2013/10/08)
An efficient and one-pot synthetic method for the regioselective ortho-nitration of the N-phenyl carboxamides and primary anilines has been developed by using bismuth nitrate and acetic anhydride as the nitrating reagents. Reaction proceeds at room temperature and results in corresponding ortho-nitrated products in moderate to excellent yields. This method provides an operationally simple, regioselective, and efficient access to synthesize o-nitro anilines under the mild conditions.
Preparation, polymerization and characterization of some new maleimides
Hiran,Paliwal,Chaudhary, Jyoti,Meena, Suresh
, p. 385 - 388 (2008/04/03)
This article described the synthesis of poly N-arylmaleimides and copolymaleimides. The maleimides monomer N- (2-nitrophenyl)maleimide (2-NPMI), N-(3-nitrophenyl)maleimide (3-NPMI) and N-(4-nitrophenyl)maleimide (4-NPMI) were prepared from corresponding s
Nitrations and Oxidations with Inorganic Nitrate Salts in Trifluoroacetic Anhydride
Crivello, J.V.
, p. 3056 - 3060 (2007/10/02)
Metal nitrates in trifluoroacetic anhydride nitrate many aromatic compounds in high yields at room temperature, including polymers with aromatic groups.However, this system oxidizes phenols to quinoid products.
