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Ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclohexanecarboxylate is a complex organic compound with the chemical formula C13H20O5. It is a derivative of cyclohexane, featuring a cyclohexane ring with a carboxylate group (-COO-) attached to the 2-position. Additionally, there is an ethyl ester group (-CH2CH3) at the 1-position, and a 2-ethoxy-2-oxoethyl group (-CH2CH3O-CO-CH2-) at the 1-position as well. This molecule is characterized by its ester and ketone functional groups, which contribute to its reactivity and potential applications in chemical synthesis. It is important to note that the compound's structure and properties should be carefully considered when evaluating its use in various chemical processes or as a reagent in organic chemistry.

7251-30-1

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7251-30-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7251-30-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,5 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7251-30:
(6*7)+(5*2)+(4*5)+(3*1)+(2*3)+(1*0)=81
81 % 10 = 1
So 7251-30-1 is a valid CAS Registry Number.

7251-30-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 1-(2-ethoxy-2-oxoethyl)-2-oxocyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names (1-Aethoxycarbonyl-2-oxo-cyclohexyl)-essigsaeure-aethylester

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7251-30-1 SDS

7251-30-1Relevant academic research and scientific papers

Syntheses of the Terpenoid Precursors Cyclopent-2-enone and Cyclohex-2-enone Diesters

Kadas, I.,Morvai, V.,Arvai, G.,Toeke, L.,Szoelloesy, A.,et al.

, p. 107 - 118 (2007/10/02)

Two reaction pathways were elaborated for the practical and convenient syntheses of the title compounds.The first route applies a bromination-dehydrobromination sequence to introduce the double bond into 1-alkoxycarbonyl-2-oxocycloalkylacetic and propioni

Surface-mediated Solid-phase Reaction. Part 2. Highly Selective Mono- and Di-C-alkylation of 1,3-Dicarbonyl Compounds on the Surface of Alumina

Ranu, Brindaban C.,Bhar, Sanjay

, p. 365 - 368 (2007/10/02)

Highly selective mono- and di-C-alkylation of 1,3-dicarbonyl compounds with different, structurally varied alkyl halides has been achieved in high yields through a simple solvent-free reaction on the surface of alumina impregnated with sodium or potassium alkoxide.

CATALYST DEPENDENT MECHANISTIC PATHS IN THE REACTIONS OF ETHYL DIAZOACETATE WITH β-KETO ESTERS

Lottes, Andrew C.,Landgrebe, John A.,Larsen, Kristin

, p. 4093 - 4096 (2007/10/02)

The catalyzed decomposition of ethyl diazoacetate in the presence of β-keto esters produces regioisomeric enol ethers and the diester from formal carbenoid insertion into the α-C-H bond.The product distribution is very catalyst dependent.

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