83629-87-2 Usage
Uses
Used in Pharmaceutical Industry:
2,3-Furandione, 4-bromo-5-phenylis used as a key intermediate in the synthesis of various pharmaceutical compounds. Its role in the Diels-Alder reaction allows for the creation of complex organic molecules that are essential in developing new drugs with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 2,3-Furandione, 4-bromo-5-phenylis utilized as a building block for the synthesis of agrochemicals, such as pesticides and herbicides. Its ability to form complex molecules through the Diels-Alder reaction contributes to the development of more effective and targeted agrochemicals.
Used in Polymer Production:
2,3-Furandione, 4-bromo-5-phenylis employed in the production of polymers, where its unique chemical properties contribute to the formation of polymers with specific characteristics. These polymers can be used in various applications, such as coatings, adhesives, and plastics.
Used as a Reagent in Chemical Processes:
Bromophenylmaleimide is used as a reagent in various chemical processes, including organic synthesis and the preparation of other chemical compounds. Its versatility and reactivity make it a valuable tool in the synthesis of a wide range of chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 83629-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,2 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 83629-87:
(7*8)+(6*3)+(5*6)+(4*2)+(3*9)+(2*8)+(1*7)=162
162 % 10 = 2
So 83629-87-2 is a valid CAS Registry Number.
83629-87-2Relevant academic research and scientific papers
CHEMISTRY OF OXALYL DERIVATIVES OF METHYL KETONES. XXXVII. SYNTHESIS AND THERMAL DECARBONYLATION OF 5-ARYL-4-HALOGENO-2,3-DIHYDRO-2,3-FURANDIONES
Andreichikov, Yu. S.,Gel't, N. V.,Kozlov, A. P.
, p. 1595 - 1600 (2007/10/02)
5-Aryl-4-halogeno-2,3-dihydro-2,3-furandiones were obtained by the halognation of 5-aryl-2,3-dihydro-2,3-furandiones.The kinetics of the thermal decarbonylation of the products, leading to the formation of 6-aryl-3-aroyl-5-bromo-4-hydroxy-2-pyranones, were investigated.A comparative assessment of the kinetics and activation parameters of the reaction indicates that the decarbonylation reaction has concerted character.
