22078-90-6 Usage
Description
(5-Phenyl-furan-2-yl)-methanol is an aromatic organic compound with the molecular formula C11H10O2. It features a furan ring fused with a phenyl group and a hydroxyl group attached to it. (5-PHENYL-FURAN-2-YL)-METHANOL serves as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Additionally, it holds promise for the development of new materials and as a starting material in the synthesis of biologically active compounds. Further research is necessary to fully explore its potential applications and properties.
Uses
Used in Pharmaceutical Industry:
(5-Phenyl-furan-2-yl)-methanol is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, (5-Phenyl-furan-2-yl)-methanol is utilized as a precursor in the production of agrochemicals, which can help in the development of more effective and environmentally friendly pesticides and other agricultural products.
Used in Material Science:
(5-Phenyl-furan-2-yl)-methanol is employed as a starting material in the development of new materials, potentially leading to advancements in various fields such as electronics, energy storage, and nanotechnology.
Used in Organic Synthesis:
As a versatile building block, (5-Phenyl-furan-2-yl)-methanol is used in organic synthesis for the creation of a wide range of organic compounds, expanding the scope of chemical research and innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 22078-90-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,7 and 8 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 22078-90:
(7*2)+(6*2)+(5*0)+(4*7)+(3*8)+(2*9)+(1*0)=96
96 % 10 = 6
So 22078-90-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H10O2/c12-8-10-6-7-11(13-10)9-4-2-1-3-5-9/h1-7,12H,8H2
22078-90-6Relevant articles and documents
A Gold-Catalyzed A3 Coupling/Cyclization/Elimination Sequence as Versatile Tool for the Synthesis of Furfuryl Alcohol Derivatives from Glyceraldehyde and Alkynes
Li, Jian,Rudolph, Matthias,Rominger, Frank,Xie, Jin,Hashmi., A. Stephen K.
, p. 207 - 211 (2016)
The reaction of glyceraldehyde with alkynes delivers furfuryl alcohol derivatives within only one reaction step in the presence of a gold(III) catalyst. The reaction cascade is initiated by an intermolecular gold-catalyzed A3 coupling sequence in which mo
Synthesis and bioactivity of phenyl substituted furan and oxazole carboxylic acid derivatives as potential PDE4 inhibitors
Lin, Yinuo,Ahmed, Wasim,He, Min,Xiang, Xuwen,Tang, Riyuan,Cui, Zi-Ning
, (2020/10/02)
In this present study, a series of 5-phenyl-2-furan and 4-phenyl-2-oxazole derivatives were designed and synthesized as phosphodiesterase type 4 (PDE4) inhibitors. In vitro results showed that the synthesized compounds exhibited considerable inhibitory ac
PREMATURE-TERMINATION-CODONS READTHROUGH COMPOUNDS
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Page/Page column 0250; 0282; 0283, (2013/10/22)
Premature termination codons readthrough compounds, composition thereof, and methods of making and using the same are provided.
