281198-93-4 Usage
Description
1-(2-(CHLOROMETHYL)-5-PHENYLFURAN-3-YL)ETHANONE is a chemical compound with the molecular formula C12H11ClO2. It is a furan derivative featuring a chloromethyl group and a phenyl group attached to the furan ring, along with an ethanone group. 1-(2-(CHLOROMETHYL)-5-PHENYLFURAN-3-YL)ETHANONE is known for its reactivity due to the presence of the chloromethyl group, making it a valuable building block or intermediate in the synthesis of other organic compounds.
Uses
Used in Pharmaceutical Industry:
1-(2-(CHLOROMETHYL)-5-PHENYLFURAN-3-YL)ETHANONE is used as a synthetic intermediate for the development of pharmaceutical compounds. Its unique structure and reactivity allow for the creation of new molecules with potential therapeutic properties, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical field, 1-(2-(CHLOROMETHYL)-5-PHENYLFURAN-3-YL)ETHANONE serves as a key intermediate in the synthesis of various agrochemical products. Its potential to be transformed into compounds with pesticidal or herbicidal properties makes it a valuable component in the development of crop protection solutions.
Used in Academic Research:
1-(2-(CHLOROMETHYL)-5-PHENYLFURAN-3-YL)ETHANONE is utilized as a research compound in academic settings. Its versatile chemical structure and reactivity make it an interesting subject for studies aimed at understanding organic reactions, exploring new synthetic routes, and discovering novel applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 281198-93-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,1,1,9 and 8 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 281198-93:
(8*2)+(7*8)+(6*1)+(5*1)+(4*9)+(3*8)+(2*9)+(1*3)=164
164 % 10 = 4
So 281198-93-4 is a valid CAS Registry Number.
281198-93-4Relevant articles and documents
Acid-catalyzed convenient transformation of 1-aryl-2-pentene-1,4-diones into polyfunctionalized furans
Onitsuka, Satoaki,Nishino, Hiroshi,Kurosawa, Kazu
, p. 3149 - 3152 (2000)
The reaction of phenylglyoxal with 2,4-pentanedione in the presence of boron trifluoride gave the unstable 3-acetyl-1-phenyl-2-pentene-1,4-dione intermediate which was converted in situ by the reaction with an excess amount of 2,4-pentanedione into new crystalline tri- and tetra-substituted furans. Other unstable 1-aryl-2-pentene-1,4-diones, which were obtained by the photooxygenation of 3-acetyl-5-aryl-2-methylfurans, were trapped by the acid-catalyzed reaction, giving polyfunctionalized furans in good yields. Treatment of the 1-phenyl-2-pentene-1,4-dione intermediate with concentrated hydrochloric acid followed by boiling ethanol quantitatively yielded a stable 2-ethoxymethylfuran via the unstable 2-chloromethylfuran. (C) 2000 Elsevier Science Ltd.
