59726-39-5 Usage
Description
Propanedioic acid, (1-Methylethyl)-2-propenyl-, diethyl ester, also known as (1-Methylethyl)-2-propenyl diethyl ester, is a chemical compound that serves as an intermediate in the synthesis of various organic compounds. It is characterized by its ester functional group and is derived from propanedioic acid.
Uses
Used in Chemical Synthesis:
Propanedioic acid, (1-Methylethyl)-2-propenyl-, diethyl ester is used as an intermediate in the synthesis of Propanedioic acid, 2-(1-methylethyl)-2-propyl-, 1,3-diethyl ester (M305005). It plays a crucial role in the cyclization of appropriate reactants, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Propanedioic acid, (1-Methylethyl)-2-propenyl-, diethyl ester is used as an intermediate in the production of barbiturate products. Barbiturates are a class of drugs that have sedative-hypnotic, anticonvulsant, and anesthetic properties, making them valuable in the treatment of various medical conditions. Propanedioic acid, (1-Methylethyl)-2-propenyl-, diethyl ester's role in the synthesis of these drugs highlights its importance in the development of therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 59726-39-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,7,2 and 6 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 59726-39:
(7*5)+(6*9)+(5*7)+(4*2)+(3*6)+(2*3)+(1*9)=165
165 % 10 = 5
So 59726-39-5 is a valid CAS Registry Number.
59726-39-5Relevant articles and documents
METHOD FOR PREPARING APRONAL AND INTERMEDIATE THEREOF
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Paragraph 0065, (2020/05/13)
PROBLEM TO BE SOLVED: To provide a simple, cost-effective and improved method for synthesizing apronal and an intermediate alkyl 2-isopropyl-4-pentenoate used in the synthesis of allylisopropylacetylurea of apronal. SOLUTION: There is provided a method including a step of reacting an alkyl 2-isopropyl-4-pentenoate with an alkali metal salt such as sodium urea in the presence of an aprotic polar solvent or a mixture of solvents to obtain apronal of the following formula (1). In addition, the present invention also includes a method for preparing the intermediate alkyl 2-isopropyl-4-pentenoate by dealkoxycarbonylation of dialkylallyl isopropyl malonate. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT
Intramolecular formal [4+2] cycloaddition of 3-ethoxycyclobutanones and alkenes
Matsuo, Jun-Ichi,Sasaki, Shun,Hoshikawa, Takaya,Ishibashi, Hiroyuki
supporting information; scheme or table, p. 934 - 936 (2010/06/12)
Intramolecular formal [4+2] cycloaddition between 3-ethoxycyclobutanones and a carbon-carbon double bond to the corresponding bicyclo[4.n.0]alkan-2-one derivatives proceeded effectively by using ethylaluminium dichloride. The Royal Society of Chemistry 20
Substituted oxotremorine derivatives and pharmaceutical use thereof
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, (2008/06/13)
This disclosure describes novel substituted oxotremorine derivatives of formula I having nitrogen, oxygen or sulfur groups and the prodrug forms of these derivatives. The compounds have cholinergic activity. Also disclosed are methods for treating disease
