923569-79-3 Usage
Uses
Used in Research Applications:
5-METHOXY-2-PERFLUOROPROPYLINDOLE is used as a research compound for studying its chemical properties, reactivity, and potential interactions with other molecules. Its unique structure allows researchers to explore its behavior in various chemical reactions and its potential as a building block for more complex organic molecules.
Used in Organic Synthesis:
In the field of organic synthesis, 5-METHOXY-2-PERFLUOROPROPYLINDOLE is used as a key intermediate or starting material for the synthesis of more complex organic compounds. Its heptafluoropropyl group and methoxyindole moiety can be further modified or used as a scaffold to create new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
5-METHOXY-2-PERFLUOROPROPYLINDOLE may also find applications in the pharmaceutical industry as a potential drug candidate or as a building block for the development of new drugs. Its unique structure and properties could be harnessed to design molecules with therapeutic potential, targeting specific biological pathways or receptors.
Used in Material Science:
In material science, 5-METHOXY-2-PERFLUOROPROPYLINDOLE could be utilized in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity. Its incorporation into polymers, coatings, or other materials could lead to innovative applications in various industries.
Overall, 5-METHOXY-2-PERFLUOROPROPYLINDOLE is a versatile compound with a wide range of potential applications across different industries, including research, organic synthesis, pharmaceuticals, and material science. Its unique structure and properties make it a valuable asset for the development of new technologies and products.
Check Digit Verification of cas no
The CAS Registry Mumber 923569-79-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,5,6 and 9 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 923569-79:
(8*9)+(7*2)+(6*3)+(5*5)+(4*6)+(3*9)+(2*7)+(1*9)=203
203 % 10 = 3
So 923569-79-3 is a valid CAS Registry Number.
923569-79-3Relevant articles and documents
A New and Efficient One-Pot Synthesis of 2-Fluoroalkyl Substituted Indoles
Wang, Zengxue,Ma, Qingwen
, p. 1893 - 1896 (2015/11/09)
A new simple and efficient one-pot synthesis of 2-fluoroalkyl substituted indoles from 2-aminobenzyl alcohols with fluorine-containing carboxylic acids in the presence of Ph3P, CCl4, and NEt3 is described. Various kinds of 2-fluoroalkyl substituted indole derivatives can be conveniently prepared.
Bromotriphenylphosphonium salt promoted one-pot cyclization to 2-fluoroalkyl-substituted indoles
Wang, Zeng-Xue,Zhang, Tai-Feng,Ma, Qing-Wen,Ni, Wei-Gui
, p. 3309 - 3314 (2015/01/09)
2-Fluoroalkyl-substituted indoles were prepared in moderate to excellent yields through bromotriphenylphosphonium salt promoted ring formation with fluorine-containing carboxylic acids in the presence of triethylamine in toluene at reflux temperature. A range of 2-fluoroalkyl-substituted indole derivatives can be conveniently prepared.
Grignard cyclization reaction of fluorinated N-arylimidoyl chlorides: A novel and facile access to 2-fluoroalkyl indoles
Ge, Fenglian,Wang, Zengxue,Wan, Wen,Hao, Jian
, p. 447 - 450 (2008/01/06)
2-Fluoroalkyl-substituted indole derivatives were simply prepared via the Grignard cyclization reaction (GCR) of corresponding fluorinated N-aryl imidoyl chlorides in good yields. This approach provides a novel and facile access to the biologically import
Fluorinated N-[2-(haloalkyl)phenyl]imidoyl chloride, a key intermediate for the synthesis of 2-fluoroalkyl substituted indole derivatives via Grignard cyclization process
Wang, Zengxue,Ge, Fenglian,Wan, Wen,Jiang, Haizhen,Hao, Jian
, p. 1143 - 1152 (2008/02/08)
Fluorinated N-[2-(haloalkyl)phenyl]imidoyl chloride, which was readily available from the corresponding anilines by using Uneyama's one-pot synthesis of fluorinated imidoyl chloride, was found to be a key intermediate for the facile synthesis of 2-fluoroa
