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195886-85-2

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195886-85-2 Usage

Physical state

Colorless liquid

Odor

Pungent

Uses

Widely used in the production of pharmaceuticals and agrochemicals

Reactivity

Highly reactive compound

Chemical reactions

Capable of undergoing various chemical reactions, including addition reactions

Role

Often used as a reagent in organic synthesis

Intermediate

Known for its role as an intermediate in the preparation of other chemical compounds, such as fluorinated derivatives

Applications

Potential applications in a variety of industries, including pharmaceuticals, agrochemicals, and organic synthesis

Safety

Important to handle with care due to potential health and environmental risks

Check Digit Verification of cas no

The CAS Registry Mumber 195886-85-2 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 5 respectively.
Calculate Digit Verification of CAS Registry Number 195886-85:
(8*1)+(7*9)+(6*5)+(5*8)+(4*8)+(3*6)+(2*8)+(1*5)=212
212 % 10 = 2
So 195886-85-2 is a valid CAS Registry Number.

195886-85-2Upstream product

195886-85-2Downstream Products

195886-85-2Relevant 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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