24079-95-6 Usage
Uses
Used in Organic Synthesis:
Ethyl 6-(isopropyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate is used as a synthetic intermediate for the preparation of various organic compounds. Its unique structure allows it to be a versatile building block in the synthesis of complex molecules, which can be further modified or functionalized for specific applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, ethyl 6-(isopropyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate is used as a key component in the development of new drugs. Its structural features can be exploited to design and synthesize bioactive molecules with potential therapeutic properties. ethyl 6-(isopropyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate may contribute to the creation of novel pharmaceutical agents targeting a range of diseases and conditions.
Used in Agrochemical Industry:
Ethyl 6-(isopropyl)-2-methyl-4-oxocyclohex-2-ene-1-carboxylate may also find applications in the agrochemical industry. It can be used as a starting material or intermediate in the synthesis of agrochemicals such as pesticides, herbicides, and insecticides. Its unique structure and reactivity can be harnessed to develop new and more effective products for agricultural use, contributing to increased crop yields and protection against pests.
Check Digit Verification of cas no
The CAS Registry Mumber 24079-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,0,7 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24079-95:
(7*2)+(6*4)+(5*0)+(4*7)+(3*9)+(2*9)+(1*5)=116
116 % 10 = 6
So 24079-95-6 is a valid CAS Registry Number.
InChI:InChI=1/C13H20O3/c1-5-16-13(15)12-9(4)6-10(14)7-11(12)8(2)3/h6,8,11-12H,5,7H2,1-4H3
24079-95-6Relevant academic research and scientific papers
Efficient preparation method of 4-hydroxybenzoic esters – Oxidation of substituted Hagemman's ester
Kang, Sein,Kim, Dahye,In, Ik Joon,Koo, Sangho
, p. 2264 - 2266 (2018/03/26)
A practical two-step synthetic method of diversely R-substituted 4-hydroxybenzoic esters, which may have wide applications in household chemicals and polymeric materials, was developed by 2:1 coupling between ethyl acetoacetate and aldehydes (RCHO) in t-BuOK/t-BuOH, followed by oxidative aromatization of the resulting Hagemman's esters. Application of the condition using stoichiometric NBS and catalytic TMS·OTf efficiently induced oxidation of the Hagemman's esters to produce 4-hydroxybenzoic esters.
Reaction of CH-acids with Michael acceptors in the presence of potassium carbonate. Syntheses of 6-acetyl- and 3,5-dialkylcyclohex-2-enones
Khachatryan,Vardapetyan,Morlyan,Razinov,Matevosyan
, p. 385 - 390 (2015/10/29)
The reaction of acetylacetone with α,β-enones in the presence of potassium carbonate affords 6-acetylcyclohex-2-enones. The assembly of two acetoacetate and one alkanal molecules gives 3,5-dialkylcyclohex-2-enones. Facile one-pot procedures for these reactions were developed.
Regio- and Stereoselectivity of the Lactone Formation via Hydrolysis of the PO-Olefination Products of α,β-Epoxycyclohexanones
Loecht, Gisela van de,Marschall, Helga,Weyerstahl, Peter
, p. 1150 - 1157 (2007/10/02)
PO-Olefination of the diastereomeric pulegone oxides 1 and 2 with 9a leads to (E,Z) esters, 1 affording mainly (E)-3, and 2 predominantly (Z)-4. (Z)-4 hydrolyzes to give a mixture of γ- and δ-lactones 6-8; whereas (Z)-3 yields stereoselectively the δ-lactone 5. - The epoxy ketone 12 reacts with 9b to give the (E,Z) ester 13. (Z)-13 stereoselectively yields the γ-lactone 14.
