62243-57-6 Usage
Uses
Used in Flavor and Fragrance Industry:
(3E)-2-methylhex-3-enoic acid is used as a flavoring agent for its distinctive fruity, slightly sour odor, enhancing the taste and aroma profiles of various food products.
Used in Pharmaceutical Development:
(3E)-2-methylhex-3-enoic acid is utilized as an active ingredient in the development of pharmaceutical products due to its potential antimicrobial and antifungal properties, contributing to the creation of new treatments and medications.
Used in Cosmetic Product Formulation:
(3E)-2-methylhex-3-enoic acid is employed as a key component in the formulation of cosmetic products, leveraging its antimicrobial and antifungal characteristics to improve product efficacy and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 62243-57-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62243-57:
(7*6)+(6*2)+(5*2)+(4*4)+(3*3)+(2*5)+(1*7)=106
106 % 10 = 6
So 62243-57-6 is a valid CAS Registry Number.
62243-57-6Relevant academic research and scientific papers
Acetoxy lactonization of alkenyl acetic acids promoted by ammonium persulfate and trifluoromethanesulfonic acid in acetic acid
Tiecco, Marcello,Testaferri, Lorenzo,Tingoli, Marco
, p. 5351 - 5358 (2007/10/02)
The reactions of substituted 4-pentenoic and 3-butenoic acids with ammonium persulfate in acetic acid, in the presence of trifluoromethanesulfonic acid, gave the products of acetoxy lactonization in good yield.
REDUCTION OF 2,4-ALKEDIENOIC ACIDS WITH SODIUM DITHIONITE
Camps, Francisco,Coll, Josep,Guitart, Josefa
, p. 185 - 194 (2007/10/02)
The reduction of sodium salts of 2,4-alkadienoic acids bearing alkyl substituents in the different positions of the diene system, in aqueous solution with sodium dithionite, affords E:Z isomeric mixtures of 3-alkenoic acids after acidification.These results are compared with those reported with those reported for the related reaction under phase transfer catalysis of the corresponding alkyl alkadienoates.Formation of sulfinic adducts as intermediates in the reduction of sorbic acid points to a two stage mechanism for the overall reduction process.
