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(4-Methoxy-2,6-dimethyl-phenyl)-(5-phenyl-tetrazol-2-yl)-methanone oxime is a complex organic compound with the molecular formula C20H19N3O2. It features a 4-methoxy-2,6-dimethylphenyl group, a 5-phenyltetrazol-2-yl group, and a methanone oxime moiety. (4-Methoxy-2,6-dimethyl-phenyl)-(5-phenyl-tetrazol-2-yl)-methanone oxime is characterized by its unique structure, which includes a phenyl ring with methoxy and methyl substituents, a tetrazol-2-yl group with a phenyl substituent, and a methanone oxime functional group. It is likely to be used in chemical research or as an intermediate in the synthesis of pharmaceuticals or other organic compounds due to its diverse functional groups and potential reactivity.

97240-84-1

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97240-84-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97240-84-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,4 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97240-84:
(7*9)+(6*7)+(5*2)+(4*4)+(3*0)+(2*8)+(1*4)=151
151 % 10 = 1
So 97240-84-1 is a valid CAS Registry Number.

97240-84-1Downstream Products

97240-84-1Relevant academic research and scientific papers

KINETICS OF THE ADDITION OF 5-ARYLTETRAZOLES TO STABLE SUBSTITUTED BENZONITRILE OXIDES

Beltrame, Paolo,Gelli, Gioanna

, p. 403 - 408 (2007/10/02)

Stable arylnitrile oxides were able to react with 5-aryltetrazoles in the presence of tertiary amine, giving open-chain addition products with the structure of 2,5-disubstituted tetrazoles.Kinetic measurements were performed at 35 deg C, mostly in chloroform in the presence of triethylamine.Substituents on the tetrazole benzene ring had almost no effect, but for substitution on the nitrile oxide benzene ring a non-Hammett-like effect was found.Rates were higher in CHCl3 than in (CHCl3 + 10percent MeOH), and with Et3N than with PhMeN.The reaction mechanism is discussed.

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