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α-Chloromethyl phenyl telluride is an organotellurium compound characterized by the presence of a chlorine atom attached to a methyl group, which is in turn bonded to a phenyl ring. This chemical structure gives it unique properties that can be exploited in various applications, such as in the synthesis of pharmaceuticals and agrochemicals. The compound is also of interest in materials science due to its potential use in the development of new semiconductor materials. Its chemical formula is C7H7ClTe, reflecting the combination of carbon, hydrogen, chlorine, and tellurium atoms. The α-chloromethyl group provides reactivity, which can be utilized in various chemical reactions, making α-chloromethyl phenyl telluride a versatile building block in organic synthesis.

95849-68-6

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95849-68-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 95849-68-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,8,4 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 95849-68:
(7*9)+(6*5)+(5*8)+(4*4)+(3*9)+(2*6)+(1*8)=196
196 % 10 = 6
So 95849-68-6 is a valid CAS Registry Number.

95849-68-6Relevant academic research and scientific papers

ALKALINE HYDROLYSIS OF DIARYL DITELLURIDES UNDER PHASE TRANSFER CONDITIONS; SYNTHESIS OF ALKYL ARYL TELLURIDES

Comasseto, J. V.,Ferreira, J. T. B.,Val, Fontanillas

, p. 261 - 266 (1984)

The disproportionation reaction of diaryl ditellurides with sodium hydroxide under phase transfer conditions at room temperature is described for the first time.The phase transfer catalyst used is 2HT-75, a trade name for a mixture of dialkyldimethylammonium chlorides.The intermediates aryl tellurolates react "in situ" with alkyl halides to give the corresponding alkyl aryl tellurides (ArTeR) in 52-72percent yield.The following compounds were prepared: Ar = C6H5, R = CH3(CH2)3CH2,(CH3)2CHCH2CH2, (CH3)2CHCH2, CH3CHBrCH2CH2, CH3(CH2)8CH2, C6H5CH2, ClCH2, C6H5CH2CH2, CH2=CHCH2, C6H5CH=CHCH2, C6H5SeCH2, ; Ar = p-CH3C6H4, R = CH3(CH2)2CH2; Ar = p-CH3OC6H4, R = CH3(CH2)2CH2; Ar = p-C2H5OC6H4, R = CH3(CH2)2CH2; Ar = 2-naphthyl, R = CH3(CH2)2CH2.

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