105003-88-1 Usage
Uses
Used in Chemical Research and Development:
2-(3-Fluoro-2-nitrophenyl)acetonitrile is utilized as a chemical intermediate for the synthesis of various organic compounds and pharmaceuticals. Its unique structure, which includes a fluorine atom, a nitro group, and a cyanide group, makes it a valuable building block in the development of new chemical entities with potential applications in medicine, materials science, and other fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(3-Fluoro-2-nitrophenyl)acetonitrile is used as a key intermediate in the synthesis of drugs with diverse therapeutic applications. Its presence in the molecular structure can influence the pharmacokinetic and pharmacodynamic properties of the resulting compounds, potentially leading to improved efficacy, selectivity, and safety profiles.
Used in Materials Science:
2-(3-Fluoro-2-nitrophenyl)acetonitrile can also be employed in the field of materials science, where it may contribute to the development of novel materials with specific properties. Its incorporation into polymers or other materials can result in altered physical, chemical, or electronic characteristics, which can be exploited in various applications, such as sensors, coatings, or advanced materials for electronics.
Check Digit Verification of cas no
The CAS Registry Mumber 105003-88-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,0 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 105003-88:
(8*1)+(7*0)+(6*5)+(5*0)+(4*0)+(3*3)+(2*8)+(1*8)=71
71 % 10 = 1
So 105003-88-1 is a valid CAS Registry Number.
105003-88-1Relevant articles and documents
Specific ortho-Cyanomethylation of Nitroarenes via the Vicarious Nucleophilic Substitution of Hydrogen
Makosza, Mieczyslaw,Wenaell, Maria,Golinski, Miroslaw,Kinowski, Andrzej
, p. 427 - 432 (2007/10/02)
The vicarious nucleophilic substitution of hydrogen in nitroarenes with acetonitrile derivatives XCH2CN in t-BuOK/THF base/solvent system proceeds exclusively ortho to the nitro group.Strong influence of substituents Z in 3-Z-nitrobenzene derivatives on the orientation has been observed.
