55327-32-7 Usage
Uses
Used in Pharmaceutical Industry:
2-(4-BROMO-PHENYL)-OXAZOLE-4-CARBALDEHYDE is used as an intermediate in the synthesis of various pharmaceuticals for its potential biological activities and medicinal applications. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of healthcare and medicine.
Used in Agrochemical Industry:
2-(4-BROMO-PHENYL)-OXAZOLE-4-CARBALDEHYDE is used as a building block in the production of agrochemicals, particularly in the development of pesticides and other agricultural chemicals. Its aromatic properties and chemical reactivity make it a valuable component in creating effective and targeted agrochemical products.
Used in Organic Synthesis:
2-(4-BROMO-PHENYL)-OXAZOLE-4-CARBALDEHYDE is used as a versatile building block in organic synthesis for its wide range of industrial and research applications. Its unique structure and reactivity enable the creation of various complex organic compounds, contributing to the advancement of chemical research and the development of new materials and products.
Check Digit Verification of cas no
The CAS Registry Mumber 55327-32-7 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 55327-32:
(7*5)+(6*5)+(5*3)+(4*2)+(3*7)+(2*3)+(1*2)=117
117 % 10 = 7
So 55327-32-7 is a valid CAS Registry Number.
55327-32-7Relevant academic research and scientific papers
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.
SUBSTITUTED BIPHENYL ISOXAZOLE SULFONAMIDES
-
, (2008/06/13)
Compounds of the formula STR1 inhibit the activity of endothelin. The symbols are defined as follows: R 1, R 2, R 3 and R 4 are each directly bonded to a ring carbon and are each independently(a) hydrogen;(b) alkyl, alkenyl, alkynyl, alkoxy,
