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Cyclohexene-1-13C is a stable isotope-labeled chemical compound, where the carbon atom at the 1-position is replaced with a carbon-13 isotope. cyclohexene-1-13C is primarily used in scientific research and chemical analysis to study the behavior of cyclohexene under various conditions, such as its reaction kinetics, metabolic pathways, and environmental fate. The presence of the 13C isotope allows for the differentiation of cyclohexene-1-13C from its natural abundance counterpart, enabling researchers to track its movement and transformations more accurately. This is particularly useful in fields such as organic chemistry, biochemistry, and environmental science, where understanding the specific interactions and transformations of molecules is crucial.

1192-09-2

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1192-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1192-09-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,9 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1192-09:
(6*1)+(5*1)+(4*9)+(3*2)+(2*0)+(1*9)=62
62 % 10 = 2
So 1192-09-2 is a valid CAS Registry Number.

1192-09-2Upstream product

1192-09-2Downstream Products

1192-09-2Relevant academic research and scientific papers

Following solid-acid-catalyzed reactions by MAS NMR spectroscopy in liquid phase - Zeolite-catalyzed conversion of cyclohexanol in water

Vjunov, Aleksei,Hu, Mary Y.,Feng, Ju,Camaioni, Donald M.,Mei, Donghai,Hu, Jian Z.,Zhao, Chen,Lercher, Johannes A.

supporting information, p. 479 - 482 (2014/01/23)

A microautoclave magic angle spinning NMR rotor is developed enabling insitu monitoring of solid-liquid-gas reactions at high temperatures and pressures. It is used in a kinetic and mechanistic study of the reactions of cyclohexanol on zeolite HBEA in 130 °C water. The 13Cspectra show that dehydration of 1-13C-cyclohexanol occurs with significant migration of the hydroxy group in cyclohexanol and the double bond in cyclohexene with respect to the 13C label. A simplified kinetic model shows the E1-type elimination fully accounts for the initial rates of 1- 13C-cyclohexanol disappearance and the appearance of the differently labeled products, thus suggesting that the cyclohexyl cation undergoes a 1,2-hydride shift competitive with rehydration and deprotonation. Concurrent with the dehydration, trace amounts of dicyclohexyl ether are observed, and in approaching equilibrium, a secondary product, cyclohexyl-1-cyclohexene is formed. Compared to phosphoric acid, HBEA is shown to be a more active catalyst exhibiting a dehydration rate that is 100-fold faster per proton. Hot analysis: The catalytic conversion of cyclohexanol on zeolite HBEA in hot liquid water leads to dehydration as well as alkylation products. A novel microautoclave suitable for application in magic angle spinning (MAS) NMR at high temperatures has been successfully applied to obtain new insight into the mechanistic pathway leading to an understanding of the reactions under selected experimental conditions.

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