65578-36-1 Usage
Description
(E)-Ethyl 3-(MethyliMino)butanoate is a chemical compound that belongs to the ester class, characterized by its molecular structure consisting of a butanoic acid derivative with an ethyl group on one end and a methylamino group on the other. (E)-ethyl 3-(MethyliMino)butanoate is known for its fruity and floral fragrance, as well as its antimicrobial properties.
Uses
Used in Pharmaceutical Industry:
(E)-Ethyl 3-(MethyliMino)butanoate is used as an intermediate in the synthesis of various pharmaceutical substances. Its antimicrobial properties make it a valuable component in the development of new drugs and treatments.
Used in Fragrance Industry:
(E)-Ethyl 3-(MethyliMino)butanoate is used as a key ingredient in the creation of fragrances due to its pleasant, fruity, and floral scent. Its unique aroma profile contributes to the development of new and innovative fragrances.
Used in Flavoring Industry:
(E)-Ethyl 3-(MethyliMino)butanoate is used as a flavoring agent in the food and beverage industry, adding a distinct and appealing taste to various products.
Used in Personal Care Products:
(E)-Ethyl 3-(MethyliMino)butanoate is used in the formulation of perfumes, lotions, and other personal care products, enhancing their scent and providing a pleasant experience for the user.
Check Digit Verification of cas no
The CAS Registry Mumber 65578-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,7 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65578-36:
(7*6)+(6*5)+(5*5)+(4*7)+(3*8)+(2*3)+(1*6)=161
161 % 10 = 1
So 65578-36-1 is a valid CAS Registry Number.
65578-36-1Relevant articles and documents
Preparation method of arbidol intermediate
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Paragraph 0022, (2020/07/02)
The invention discloses a preparation method of an arbidol intermediate. Ethyl acetoacetate, monomethylamine and p-benzoquinone used as initial raw materials undergo methylation, cyclization, acetylation, bromination and benzene vulcanization to prepare the target compound ethyl 5-hydroxy-6-bromo-2-phenylthiomethyl-1-methylindole-3-carboxylate. The preparation method of the arbidol intermediate issimple and convenient to operate, cheap and easily available in raw materials, high in yield, low in cost, good in quality, environment-friendly, mild in reaction condition, high in safety productioncoefficient and suitable for large-scale industrial production.
Ring Cleavage Reactions of 3- and 5-Non-substituted Isoxazoles
Alberola, A.,Gonzalez, A. M.,Guerra, D.,Pulido, F. J.
, p. 1073 - 1076 (2007/10/02)
5-Methylisoxazoles with electron-accepting groups at C-4 (Ia-c) and 2,3-dimethylisoxazolium iodide (II) undergo ring cleavage when treated with organic bases.The nature of the open chain products which were obtained (stable enolates, β-diketones, esters) depends on the group at C-4 and the strength of the base.In some of these processes aromatic aldehydes were used in order to determine the competition between the condensation and the cleavage reaction.The mechanism of the nucleophilic ring cleavage of II is also shown.
