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Cyclobutane, 1,1-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18931-71-0

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18931-71-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18931-71-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,3 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18931-71:
(7*1)+(6*8)+(5*9)+(4*3)+(3*1)+(2*7)+(1*1)=130
130 % 10 = 0
So 18931-71-0 is a valid CAS Registry Number.

18931-71-0Downstream Products

18931-71-0Relevant academic research and scientific papers

ZEOLITIC CATALYTIC CONVERSION OF ALCOHOLS TO HYDROCARBONS

-

Page/Page column 19, (2013/02/28)

A method for converting an alcohol to a hydrocarbon, the method comprising contacting said alcohol with a metal-loaded zeolite catalyst at a temperature of at least 100°C and up to 550°C, wherein said alcohol can be produced by a fermentation process, said metal is a positively-charged metal ion, and said metal-loaded zeolite catalyst is catalytically active for converting said alcohol to said hydrocarbon.

The Kinetics and Mechanism of Ring Opening of Radicals containing the Cyclobutylcarbinyl System

Beckwith, Athelstan L. J.,Moad, Graeme

, p. 1083 - 1092 (2007/10/02)

The kinetic parameters of β-fission of radicals containing the cyclobutylcarbinyl system have been determined by analysis of the mixtures obtained when suitable chloro-compounds are treated with tributylstannane.Under these conditions ring opening is irreversible and in the rigid bicyclic system (4) is under stereoelectronic control.For ring opening of cyclobutylcarbinyl radical (8) kf = 4.3 x 103 s-1 at 60 deg C, and the best values of the activation parameters appear to be ΔH(excit.) = 12.2 kcal mol-1 and ΔS(excit.) = -7.4 cal mol-1 K-1.Monocyclic systems undergo preferential fission of the more substituted βγ-bond.Methyl substituents at the α-, β-, or δ-positions have little effect but γ-substitution strongly enhances the rate of ring opening.The transition state is reactant-like and has a similar disposition of centres to that (1) for homolytic addition.

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