5554-99-4 Usage
Uses
Used in Advanced Materials:
(2-Methyl-3-furyl)methanol is used as a building block in the synthesis of advanced materials for various applications, such as polymers, resins, and coatings. Its unique chemical structure contributes to the properties of these materials, enhancing their performance and durability.
Used in Industrial Chemical Processes:
(2-Methyl-3-furyl)methanol serves as an intermediate in the production of various industrial chemicals. Its reactivity and functional groups make it a valuable component in the synthesis of other compounds, contributing to the development of new products and processes.
Used in Pharmaceutical Industry:
(2-Methyl-3-furyl)methanol has potential applications in the pharmaceutical industry, where it may be used as an active pharmaceutical ingredient or as a key intermediate in the synthesis of drug molecules. Its unique structure and properties could contribute to the development of new therapeutic agents with novel mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 5554-99-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,5 and 4 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5554-99:
(6*5)+(5*5)+(4*5)+(3*4)+(2*9)+(1*9)=114
114 % 10 = 4
So 5554-99-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H8O2/c1-5-6(4-7)2-3-8-5/h2-3,7H,4H2,1H3
5554-99-4Relevant academic research and scientific papers
Dearomatization of furans via [2,3]-Still-Wittig rearrangement
Caruana, Patrick A.,Frontier, Alison J.
, p. 10921 - 10926 (2007/10/03)
Furans and benzofurans of type 1 were dearomatized via the [2,3]-Still-Wittig rearrangement. Enol ethers 2 could be isolated or isomerized to the corresponding furans 3. The substitution pattern at the homofuranylic position had a strong influence on reaction behavior. Benzofurans rearranged with the greatest efficiency, and employment of a 3-substituted benzofuran (1; R′=CH3) allowed the creation of a quaternary carbon center.
