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32675-48-2

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32675-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 32675-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,6,7 and 5 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 32675-48:
(7*3)+(6*2)+(5*6)+(4*7)+(3*5)+(2*4)+(1*8)=122
122 % 10 = 2
So 32675-48-2 is a valid CAS Registry Number.

32675-48-2Downstream Products

32675-48-2Relevant articles and documents

A kinetic study of the high temperature rearrangement of 4-ethyl-3,5-diphenyl-4H-1,2,4-triazole

Gautun,Carlsen

, p. 955 - 959 (2001)

The kinetics of the thermal rearrangement 4-ethyl-3,5-diphenyl-4H-1,2,4-triazoles, 1, to the corresponding 1-ethyl-3,5-diphenyl-l-alkyl-1H-1,2,4-triazoles, 2, was studied in 15-Crown-5 and octadecane at 3130 °C. The reaction was very slow in octadecane but proceed well in 15-Crown-5. The reaction order for the reaction was not constant but changed from an initial second order rate law towards a first order rate law as the reaction progressed. This was confirmed by the concentration dependent reaction order, nc, which was larger than the time dependent rate law, nt. The rationale for the observation was, that at high substrate concentrations the reaction order was second order while at lower concentrations a competing solvent assisted reaction plays an increasing important role. The data were in agreement with a mechanism in which the neutral 4-alkyl-triazoles in an intermolecular nucleophilic displacement reaction form a triazolium triazolate, which in a subsequent nucleophilic reaction gives the observed product.

Thermal rearrangement of 4-alkyl-4H-1,2,4-triazoles to 1-alkyl-1H-1,2,4-triazoles - A study of the mechanism by cross-over experiments

Gautun, Odd R.,Carlsen, Per H. J.

, p. 3745 - 3748 (2007/10/03)

The mechanism for the thermal rearrangement of 4-alkyl-1,2,4-triazoles to the corresponding 1-alkyl-1,2,4-triazoles, was studied by cross-over experiments with mixtures of 4-ethyl-3,5-diphenyl-4H-1,2,4-triazole and 3,5-bis(4-methylphenyl)-4-propyl-4H-1,2,

Substituent Effects in the Rearrangement of 4-Alkyl-4H-1,2,4-triazoles

Gautun, Odd Reidar,Carlsen, Per H. J.

, p. 411 - 416 (2007/10/02)

A study of the thermal rearrangement of neat 4-alkyl-substituted 4H-1,2,4-triazoles to the corresponding 1-alkyl-1H-1,2,4-triazoles showed that the rearrangement was accompanied by formation of 3,5-diphenyl-1H-1,2,4-triazole and alkenes.The composition of

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