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2-methyl-5-ethyl-5-methylcyclohexane-1,3-dione is a complex organic compound with the molecular formula C10H16O2. It is a cyclic ketone, characterized by the presence of two carbonyl groups (C=O) at positions 1 and 3 of the cyclohexane ring. The structure also includes a methyl group (CH3) at position 2, an ethyl group (C2H5) at position 5, and another methyl group at position 5. 2-methyl-5-ethyl-5-methylcyclohexane-1,3-dione is a derivative of cyclohexane, with the addition of these functional groups altering its chemical properties and reactivity. It is an example of a substituted cyclohexane, which can be found in various chemical and industrial applications, although specific uses for this particular compound are not widely documented.

1197-86-0

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1197-86-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197-86-0 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 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1197-86:
(6*1)+(5*1)+(4*9)+(3*7)+(2*8)+(1*6)=90
90 % 10 = 0
So 1197-86-0 is a valid CAS Registry Number.

1197-86-0Downstream Products

1197-86-0Relevant academic research and scientific papers

Aluminum Chloride-Mediated Dieckmann Cyclization for the Synthesis of Cyclic 2-Alkyl-1,3-alkanediones: One-Step Synthesis of the Chiloglottones

Armaly, Ahlam M.,Bar, Sukanta,Schindler, Corinna S.

supporting information, p. 3958 - 3961 (2017/08/15)

Cyclic 2-alkyl-1,3-alkanediones are ubiquitous structural motifs in many natural products of biological importance. Reported herein is an AlCl3·MeNO2-mediated Dieckmann cyclization reaction of general synthetic utility that enables direct access to complex 2-alkyl-1,3-dione building blocks from readily available dicarboxylic acid and acid chloride substrates. This new strategy enables direct synthetic access to the chiloglottone plant pheromones from commercial material in a single synthetic transformation.

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