10577-96-5 Usage
Uses
Used in Polymer Production:
4,5-dihydro-2-vinyl-1H-imidazole is used as a monomer for the synthesis of polymers, specifically polyimides and polyamides. Its incorporation into these polymers enhances their properties, such as thermal stability and mechanical strength, making them suitable for various high-performance applications.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 4,5-dihydro-2-vinyl-1H-imidazole serves as a key building block in the development of new drugs. Its reactivity allows for the creation of diverse chemical structures with potential therapeutic properties, contributing to the discovery of novel medications.
Used in Organic Synthesis:
4,5-dihydro-2-vinyl-1H-imidazole is utilized as a versatile intermediate in organic synthesis. Its ability to undergo various chemical reactions makes it a valuable component in the preparation of a wide array of organic compounds for different applications, including agrochemicals, dyes, and other specialty chemicals.
It is crucial to handle 4,5-dihydro-2-vinyl-1H-imidazole with care due to its potential health hazards and environmental impact, ensuring safe practices in its production, use, and disposal.
Check Digit Verification of cas no
The CAS Registry Mumber 10577-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 10577-96:
(7*1)+(6*0)+(5*5)+(4*7)+(3*7)+(2*9)+(1*6)=105
105 % 10 = 5
So 10577-96-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H8N2/c1-2-5-6-3-4-7-5/h2H,1,3-4H2,(H,6,7)
10577-96-5Relevant academic research and scientific papers
Microwave-assisted facile synthesis of 2-substituted 2-imidazolines
Pathan, Mohsin Y.,Paike, Vijaykumar V.,Pachmase, Pandurang R.,More, Sandeep P.,Ardhapure, Suresh S.,Pawar, Rajendra P.
, p. 205 - 210 (2013/09/12)
A novel method for the synthesis of 2-substituted 2-imidazolines under microwave irradiation is reported. The yields of product obtained using this protocol are significantly high and the reaction time is reduced. ARKAT.
Process for preparation of 2-vinylimidazolines
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, (2008/06/13)
2-vinyl-2-imidazolines are prepared by cleaving 2-acylamidoethyl-2-imidazolines at suitable temperature, distilling the cleavage products, and recovering the desired product from the distillate.
Process for preparing unsaturated imidazolines
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, (2008/06/13)
Compounds having the formula STR1 wherein R1 is hydrogen or methyl and R2 , R3 and R4 are, individually, hydrogen, alkyl (C1 -C4), aryl (C6 -C10), aralkyl (C7 -C11) or alkaryl (C7 -C11) are prepared by heating hydroxyethyl or hydrocarbyloxyethyl imidazolines at 275°-500° and in the presence of a catalyst. Salts are also prepared.
Unsaturated imidazolines
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, (2008/06/13)
Compounds having the formula STR1 wherein n and m are, individually, 0 or 1, X is an anion, R' is hydrogen, methyl or phenyl and R2, R3 and R4 are, individually, hydrogen, alkyl, aryl, alkaryl or aralkyl, polymers thereof and methods for their production, are disclosed. The compounds form polymers useful in the treatment of water sludges, the formation of fibers and the treatment of paper.
