95729-22-9 Usage
Uses
Used in Fragrance Industry:
5-Fluoro-2-methylanisole is used as a fragrance ingredient for its sweet, floral scent, adding unique aroma profiles to various products in the fragrance industry.
Used in Flavor Industry:
In the flavor industry, 5-Fluoro-2-methylanisole serves as a flavoring agent, enhancing the taste and aroma of food and beverage products.
Used in Pharmaceutical Synthesis:
5-Fluoro-2-methylanisole is utilized in the synthesis of pharmaceuticals, contributing to the development of new drugs and medicinal compounds.
Used in Agrochemical Synthesis:
5-FLUORO-2-METHYLANISOLE also plays a role in the synthesis of agrochemicals, aiding in the creation of products for agricultural applications such as pesticides and fertilizers.
Check Digit Verification of cas no
The CAS Registry Mumber 95729-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,7,2 and 9 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 95729-22:
(7*9)+(6*5)+(5*7)+(4*2)+(3*9)+(2*2)+(1*2)=169
169 % 10 = 9
So 95729-22-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO/c1-6-3-4-7(9)5-8(6)10-2/h3-5H,1-2H3
95729-22-9Relevant academic research and scientific papers
4,5-Dimethyl-2-Iodoxybenzenesulfonic Acid Catalyzed Site-Selective Oxidation of 2-Substituted Phenols to 1,2-Quinols
Uyanik, Muhammet,Mutsuga, Tatsuya,Ishihara, Kazuaki
supporting information, p. 3956 - 3960 (2017/03/27)
A site-selective hydroxylative dearomatization of 2-substituted phenols to either 1,2-benzoquinols or their cyclodimers, catalyzed by 4,5-dimethyl-2-iodoxybenzenesulfonic acid with Oxone, has been developed. Natural products such as biscarvacrol and lacinilene C methyl ether could be synthesized efficiently under mild reaction conditions. Furthermore, both the reaction rate and site selectivity could be further improved by the introduction of a trialkylsilylmethyl substituent at the 2-position of phenols. The corresponding 1,2-quinols could be transformed into various useful structural motifs by [4+2] cycloaddition cascade reactions.
