181765-84-4 Usage
Uses
Used in Pharmaceutical Industry:
[(S)-2-(3,4-Dichloro-phenyl)-pent-4-en-(E)-ylidene]-ethyl-amine is used as a potential active pharmaceutical ingredient for [application reason] due to its unique chemical structure and chiral properties. Its specific stereochemistry may allow for targeted drug design and development, potentially leading to more effective treatments with fewer side effects.
Used in Agrochemical Industry:
In the agrochemical sector, [(S)-2-(3,4-Dichloro-phenyl)-pent-4-en-(E)-ylidene]-ethyl-amine is used as a key component in the development of novel pesticides or herbicides for [application reason]. Its chemical properties may contribute to the creation of more effective and environmentally friendly solutions for agricultural challenges.
Used in Chemical Research:
[(S)-2-(3,4-Dichloro-phenyl)-pent-4-en-(E)-ylidene]-ethyl-amine serves as a valuable compound in chemical research and development for [application reason]. Its unique structure and properties make it an interesting subject for studying various chemical reactions and potential applications in material science or other specialized fields.
Check Digit Verification of cas no
The CAS Registry Mumber 181765-84-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,1,7,6 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 181765-84:
(8*1)+(7*8)+(6*1)+(5*7)+(4*6)+(3*5)+(2*8)+(1*4)=164
164 % 10 = 4
So 181765-84-4 is a valid CAS Registry Number.
181765-84-4Relevant academic research and scientific papers
Campbell, James B.,Dedinas, Robert F.,Trumbower-Walsh, Sally A.
, p. 6205 - 6211 (1996)
Addition of phenyllithium to a mixture of an imine, methyl o-iodobenzoate, and BF3-etherate at -105°C gives good to excellent yields of isoindolones. The transient formation of methyl o-lithiobenzoate is proposed, which is formed by a rapid lithium/iodide exchange reaction of the phenyllithium with methyl o-iodobenzoate in the presence of the imine. The transiently generated anions can then be captured by the BF3-activated imines to form the isoindolones in good to high yield. The reactions conditions are sufficiently mild, and selective, to permit functional groups such carbmethoxy and aryl bromide, which could otherwise react with the added PhLi, to be tolerated.
