13670-33-2 Usage
Uses
Used in Flavor and Fragrance Industry:
4,5-Dihydrooxazole, 2-vinylis used as a flavor and fragrance agent in the food and cosmetic industries. Its strong odor makes it a valuable component in creating various scents and flavors, enhancing the sensory experience of products.
Used in Pharmaceutical Production:
4,5-Dihydrooxazole, 2-vinylis also utilized in the production of pharmaceuticals. Its unique chemical structure allows it to serve as a building block in the synthesis of various drugs, contributing to the development of new medications with potential therapeutic benefits.
Used in Organic Synthesis:
4,5-Dihydrooxazole, 2-vinylis employed as a building block in organic synthesis. Its versatile chemical properties enable it to be incorporated into the synthesis of a wide range of organic compounds, facilitating the creation of new molecules with diverse applications.
Used in Anti-Inflammatory and Antimicrobial Applications:
4,5-Dihydrooxazole, 2-vinylhas been studied for its potential biological activities, including its use as an anti-inflammatory and antimicrobial agent. Its ability to modulate inflammatory responses and inhibit the growth of microorganisms makes it a promising candidate for the development of new treatments in these areas.
Check Digit Verification of cas no
The CAS Registry Mumber 13670-33-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13670-33:
(7*1)+(6*3)+(5*6)+(4*7)+(3*0)+(2*3)+(1*3)=92
92 % 10 = 2
So 13670-33-2 is a valid CAS Registry Number.
13670-33-2Relevant academic research and scientific papers
Synthesis of 2-Vinyl-2-oxazoline by Isomerisation of N-Acryloylaziridine
Woo, H.G.
, p. 1114 (2007/10/02)
2-Vinyl-2-oxazoline (3) is quantitatively obtained by the isomerisation of N-acryloylaziridine (1) at room temperature in the presence of potassium thiocyanate in dimethyl sulphoxide-hexamethylphosphoric acid triamide (HMPT)(9:1, v/v).It is found that the introduction of electron-withdrawing substituent into acryloyl group facilitates the isomerisation reaction.
Process for making 2-vinyl-2-oxazolines
-
, (2008/06/13)
2-Vinyl-2-oxazolines are prepared in the novel process comprising reacting (1) an N-(2-haloalkyl)-3-halopropionamide with (2) at least 2 equivalents of an inorganic base per mole of (1). The process is conducted under substantially anhydrous conditions and in the presence of an alkylene glycol or a polyalkylene glycol.
