23251-67-4 Usage
Uses
Used in Organic Synthesis:
(5Z)-5-hex-2-yn-1-ylidenefuran-2(5H)-one is used as a key intermediate in organic synthesis for the development of novel compounds with potential applications in various industries. Its unique structure allows for versatile chemical reactions, enabling the synthesis of a wide range of molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (5Z)-5-hex-2-yn-1-ylidenefuran-2(5H)-one is used as a building block for the design and synthesis of new pharmaceutical agents. Its distinct structural features may contribute to the discovery of innovative drugs with improved therapeutic properties and reduced side effects.
Used in Chemical Research:
(5Z)-5-hex-2-yn-1-ylidenefuran-2(5H)-one serves as a valuable subject for chemical research, providing insights into the reactivity and properties of heterocyclic aromatic compounds. Studying (5Z)-5-hex-2-yn-1-ylidenefuran-2(5H)-one can lead to a better understanding of its potential applications and the development of new synthetic methods and strategies.
Used in Material Science:
(5Z)-5-hex-2-yn-1-ylidenefuran-2(5H)-one has potential applications in material science, where its unique structure and properties can be utilized to develop new materials with specific characteristics. These materials could find use in various industries, such as electronics, coatings, and adhesives.
Check Digit Verification of cas no
The CAS Registry Mumber 23251-67-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,5 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23251-67:
(7*2)+(6*3)+(5*2)+(4*5)+(3*1)+(2*6)+(1*7)=84
84 % 10 = 4
So 23251-67-4 is a valid CAS Registry Number.
23251-67-4Relevant academic research and scientific papers
SYNTHESIS OF 4-YLIDENEBUTENOLIDES FROM 2-TRIMETHYLSILOXYFURAN
Asaoka, Morio,Yanagida, Noboru,Ishibashi, Keiji,Takei, Hisashi
, p. 4269 - 4270 (2007/10/02)
Dehydration or dealkoxylation of the reaction products of various aldehydes, ketones, and acetals with 2-trimethylsiloxyfuran gave corresponding 4-ylidenebutenolides in good to high overall yields.
