80141-91-9 Usage
Description
4-Fluoro-2-methylbenzyl alcohol, with the chemical formula C8H9FO, is an organic compound characterized by its colorless liquid state and a mild aromatic odor. It is recognized for its versatile chemical properties, making it a valuable building block in the synthesis of various organic compounds, pharmaceuticals, and agrochemicals.
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-Fluoro-2-methylbenzyl alcohol is used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals for its ability to contribute to the development of new and effective products in these fields.
Used as a Solvent in Organic Synthesis:
4-Fluoro-2-methylbenzyl alcohol is utilized as a solvent in organic synthesis due to its mild antiseptic properties and its capacity to facilitate chemical reactions, making it a preferred choice for various laboratory and industrial processes.
Used in Fragrance Industry:
4-Fluoro-2-methylbenzyl alcohol is employed as a fragrance ingredient in perfumes and personal care products, capitalizing on its aromatic scent to enhance the appeal of these consumer goods.
Check Digit Verification of cas no
The CAS Registry Mumber 80141-91-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,1,4 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80141-91:
(7*8)+(6*0)+(5*1)+(4*4)+(3*1)+(2*9)+(1*1)=99
99 % 10 = 9
So 80141-91-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO/c1-6-4-8(9)3-2-7(6)5-10/h2-4,10H,5H2,1H3
80141-91-9Relevant articles and documents
Catalytic Asymmetric (3 + 3) Cycloaddition of Oxyallyl Zwitterions with α-Diazomethylphosphonates
Liu, Yan,Peng, Xian,Peng, Yungui,She, Rui,Zhou, Xin
, p. 7295 - 7300 (2021/10/01)
The unique structure of oxyallyls represents a significant challenge for their catalytic asymmetric applications. Herein, an unprecedented chiral imidodiphosphoric acid-catalytic enantioselective (3 + 3) cycloaddition between oxyallyl zwitterions generate
PYRROLOY2,3-c¨PYRIDINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND USE
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Page/Page column 45, (2010/11/27)
Provision of a compound having a superior proton pump action, which shows an antiulcer activity and the like after conversion to an in vivo proton pump inhibitor, a production method thereof and use thereof. A pyrrolo[2,3-c]pyridine compound represented by the formula: wherein each symbol is as defined in the specification.
