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Ethyl 2,2-dimethyl-4,6-dioxocyclohexanecarboxylate is a chemical compound with the molecular formula C11H16O4. It is a white crystalline solid that is soluble in organic solvents. ethyl 2,2-dimethyl-4,6-dioxocyclohexanecarboxylate is a derivative of cyclohexane, featuring a carboxylate group attached to the ethyl ester. It is synthesized through a series of chemical reactions, including the oxidation of a cyclohexane derivative. Ethyl 2,2-dimethyl-4,6-dioxocyclohexanecarboxylate is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain antibiotics and insecticides. Its structure provides a rigid cyclic backbone, which is valuable for the development of compounds with specific biological activities.

4029-25-8

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4029-25-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4029-25-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,2 and 9 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4029-25:
(6*4)+(5*0)+(4*2)+(3*9)+(2*2)+(1*5)=68
68 % 10 = 8
So 4029-25-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H16O4/c1-4-15-10(14)9-8(13)5-7(12)6-11(9,2)3/h9H,4-6H2,1-3H3

4029-25-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2,2-dimethyl-4,6-dioxocyclohexane-1-carboxylate

1.2 Other means of identification

Product number -
Other names EINECS 223-713-0

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:4029-25-8 SDS

4029-25-8Relevant academic research and scientific papers

ORGANIC REACTIONS AT HIGH PRESSURE. MICHAEL ADDITION OF ACTIVATED ACYCLIC DONORS WITH β,β-DISUBSTITUTED ENONE ACCEPTORS.

Dauben, William G.,Gerdes, John M.

, p. 3841 - 3844 (2007/10/02)

High pressure, 15 kbar (1.5 GPa) Michael additions of doubly activated acyclic donors to sterically hindered enone acceptors with 1,5-diazabicyclonon-5-ene in acetonitrile affords Michael adducts in 42-82percent yield.

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