55327-30-5 Usage
Uses
Used in Pharmaceutical Industry:
2-P-TOLYL-OXAZOLE-4-CARBALDEHYDE is used as a building block for the preparation of various organic compounds with potential bioactive properties. Its unique chemical structure allows it to be a promising candidate for the development of new pharmaceuticals.
Used in Agrochemical Industry:
2-P-TOLYL-OXAZOLE-4-CARBALDEHYDE is used as a starting material for the synthesis of agrochemicals. Its unique chemical structure and properties may contribute to the development of new and effective agrochemicals.
Used in Materials Science:
2-P-TOLYL-OXAZOLE-4-CARBALDEHYDE is used as a component in the development of new materials with specific properties. Its unique chemical structure may contribute to the creation of advanced materials for various applications.
Used as a Reagent in Chemical Synthesis:
2-P-TOLYL-OXAZOLE-4-CARBALDEHYDE is used as a reagent in chemical synthesis and organic transformations. Its unique chemical structure and properties make it a valuable tool for chemists in the synthesis of various organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 55327-30-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,2 and 7 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 55327-30:
(7*5)+(6*5)+(5*3)+(4*2)+(3*7)+(2*3)+(1*0)=115
115 % 10 = 5
So 55327-30-5 is a valid CAS Registry Number.
55327-30-5Relevant academic research and scientific papers
O-Transfer-facilitated cyclizations of propargylamides with TMSN3: Selective synthesis of tetrazoles and dihydroimidazoles
Hu, Yancheng,Yi, Ruxia,Yu, Xinzhang,Xin, Xiaoyi,Wang, Chunxiang,Wan, Boshun
supporting information, p. 15398 - 15401 (2015/10/20)
An unprecedented formal [3+2] annulation of propargylamides with TMSN3 to deliver functionalized tetrazoles is developed. Oxygen-atom transfer (OAT) from the amide group to the CC bond was realized via a NIS-triggered-cyclization/ring-opening cascade pathway. The OAT process enables the amide to serve as a two-atom unit in the reactions. Notably, in situ umpolung of azide occurred when terminal propargylamides were employed in this reaction, providing an array of diiodomethylated dihydroimidazoles.
Thermal rearrangement of azido ketones into oxazoles via azirines: One-pot, metal-free heteroannulation to functionalized 1,3-oxazoles
Shah, Shailesh R.,Navathe, Sudhanva S.,Dikundwar, Amol G.,Guru Row, Tayur N.,Vasella, Andrea T.
supporting information, p. 264 - 267 (2013/02/26)
α-Azidoacetophenones were converted into 2-aryl-1,3-oxazole-4- carbaldehydes through rearrangement of the carbon framework upon exposure to DMF/POCl3. The unprecedented rearrangement occurs via alkenyl azides and 2H-azirines. A mechanism for this unusual reaction was proposed and evidenced.
