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195886-83-0

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195886-83-0 Usage

Physical state

Colorless liquid

Odor

Strong, sweet

Usage

Building block in the synthesis of other organic compounds

Classification

Hazardous substance

Health hazards

Causes irritation to eyes, skin, and respiratory system

Flammability

Flammable

Handling precautions

Handle with caution

Chemical structure

Cyclohexadiene ring with three fluorine atoms and a methyl group attached

Reactivity

Unique properties and reactivity due to its chemical structure

Importance

Important chemical intermediate in the field of organic chemistry

Potential applications

Range of potential applications in organic chemistry

Check Digit Verification of cas no

The CAS Registry Mumber 195886-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,5,8,8 and 6 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 195886-83:
(8*1)+(7*9)+(6*5)+(5*8)+(4*8)+(3*6)+(2*8)+(1*3)=210
210 % 10 = 0
So 195886-83-0 is a valid CAS Registry Number.

195886-83-0Upstream product

195886-83-0Downstream Products

195886-83-0Relevant articles and documents

Competitive fluorination on methyl-group and benzene-ring during the anodic fluorination of fluorotoluenes in Et4NF · mHF

Momota, Kunitaka,Yonezawa, Tetsuo,Mukai, Katsuji,Morita, Masayuki

, p. 173 - 178 (2007/10/03)

Electrochemical fluorinations of 2-fluorotoluene (2a), 3-fluorotoluene (3a) and 4-fluorotoluene (4a) in neat Et4NF · mHF (Et = C2H5, m = 3.5 or 4.0) were carried out on a platinum anode. The fluorination of 2a, 3a and 4a occurred competitively both on the side-chain (formation of monofluoromethylfluorobenzenes) and on the benzene-ring (formation of methyltrifluoro-1,4-cyclohexadienes). These results are explained by the facility of proton elimination from the methyl groups of the radical cations which have been formed by the anodic one-electron transfer reactions of 2a, 3a and 4a. A cyclic voltammogram of 4a showed three anodic current peaks which correspond to the oxidation of 4a, 1-fluoromethyl-4-fluorobenzene (4b) and 1-difluoromethyl-4-fluorolbenzene (4c). On the other hand, voltammograms of 2a and 3a showed two anodic current peaks and no difluoromethylfluorobenzenes was obtained during the fluorination of 2a and 3a.

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