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451-80-9

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451-80-9 Usage

General Description

2-Fluorophenetole, also known as 1-fluoro-2-methoxybenzene, is a colorless liquid aromatic compound with the chemical formula C8H9FO. It is commonly used as an intermediate for the synthesis of pharmaceuticals and agrochemicals. 2-Fluorophenetole has a sweet, floral odor and is often used as a fragrance ingredient in perfumes and other personal care products. It is also used as a solvent and as a chemical intermediate in organic synthesis. The compound is considered to be a flammable liquid, and proper safety precautions should be taken when handling or storing it.

Check Digit Verification of cas no

The CAS Registry Mumber 451-80-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,5 and 1 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 451-80:
(5*4)+(4*5)+(3*1)+(2*8)+(1*0)=59
59 % 10 = 9
So 451-80-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H9FO/c1-2-10-8-6-4-3-5-7(8)9/h3-6H,2H2,1H3

451-80-9Downstream Products

451-80-9Relevant articles and documents

A new alkylation of aryl alcohols by boron trifluoride etherate

Jumbam, Ndze Denis,Maganga, Yamkela,Masamba, Wayiza,Mbunye, Nomthandazo I.,Mgoqi, Esethu,Mtwa, Sphumusa

, (2019/10/28)

The ethylation of aryl alcohols by an ethyl moiety of boron trifluoride etherate is described. The reaction proceeded cleanly and afforded good yields of the corresponding aryl ethyl ethers. It tolerated the presence of functional groups such as aryl, alkyl, halogens, nitro, nitrile, and amino. However, the presence of amino or nitro groups ortho to a hydroxyl group of an aryl compound drastically reduced the yields of the anticipated products due to the chelation of the aforementioned functional groups with boron trifluoride etherate. A nitrogen atom in the aromatic ring system, as exemplified by hydroxypyridine and 8-hydroxyquinoline, completely inhibited the reaction. Resorcinol, hydroquinone, and aryl alcohols with aldehyde functions decomposed under the reaction conditions.

Synthesis of aryl fluorides from potassium aryltrifluoroborates and selectfluor mediated by iron(III) chloride

Dubbaka, Srinivas Reddy,Gadde, Satyanarayana,Narreddula, Venkateswara Reddy

, p. 854 - 860 (2015/03/14)

The synthesis of fluorinated arenes by the iron-mediated fluorination of potassium aryltrifluoroborates with Selectfluor and potassium fluoride is described. The fluorination reaction uses commercially available reagents and without requiring the addition

Preparation process of fluorine substituted aromatic compound

-

, (2008/06/13)

A preparation process of a fluorine substituted aromatic compound comprising reacting an alkali metal or alkali earth metal salt of an aromatic compound having a hydroxy group with an organic fluorinating agent is disclosed. As a representative fluorinating agent, a bis-dialkylamino-difluoromethane compound, for example, 2,2′-difluoro-1,3-dimethylimidazolidine, is exemplified. According to the process, an industrially useful fluorinated aromatic compound, for example, a fluorobenzene, a fluorine substituted benzophenone, a fluorine substituted diarylsulfone can be prepared with ease in economy without specific equipment.

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