66227-85-8 Usage
Uses
Used in Pharmaceutical Industry:
(E)-N'-(6-Methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)benzenesulfonohydrazide is used as an active pharmaceutical ingredient for its potential therapeutic effects. Its unique structure may allow it to interact with biological targets, possibly leading to the development of new drugs for various medical conditions.
Used in Agrochemical Industry:
In the agrochemical sector, (E)-N'-(6-Methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)benzenesulfonohydrazide is used as a chemical intermediate for the synthesis of various pesticides and other agrochemical products. Its properties may contribute to the development of more effective and environmentally friendly solutions for pest control and crop protection.
Used in Materials Science:
Within the field of materials science, (E)-N'-(6-Methoxy-3,4-dihydronaphthalen-1(2H)-ylidene)benzenesulfonohydrazide is utilized as a component in the development of novel materials. Its chemical properties may be harnessed to create advanced materials with specific characteristics, such as improved stability, reactivity, or other desirable traits for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 66227-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,2 and 7 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 66227-85:
(7*6)+(6*6)+(5*2)+(4*2)+(3*7)+(2*8)+(1*5)=138
138 % 10 = 8
So 66227-85-8 is a valid CAS Registry Number.
66227-85-8Relevant academic research and scientific papers
Silanes in Organic Synthesis. 8. Preparation of Vinylsilanes from Ketones and Their Regiospecific Cyclopentenone Annulation
Paquette, Leo A.,Fristad, William E.,Dime, David S.,Bailey, Thomas R.
, p. 3017 - 3028 (2007/10/02)
A general method is described for the formation of vinylsilanes from ketones.Thus, conversion to the benzene- or p-toluenesulfonylhydrazone and sequential treatment with n-butyllithium and chlorotrimethylsilane in anhydrous tetramethylethylenediamine proceeds regiospecifically to afford the less substituted vinylsilane (in unsymmetrical cases).Friedel-Crafts acylation with acryloyl chlorides and aluminium chloride and subsequent Nazarov cyclization with Lewis acid catalysis results in cyclopentenone annulation.Numerous examples that reveal the scope of this processare described.Due to accompanying polymerization, annulation with acryloyl chloride itself is least efficient.This complication can, however, be averted through use of β-chloropropionyl chloride and dehydrochlorination with 1,5-diazabicycloundec-5-ene prior to ring closure.
