2396-78-3 Usage
Description
Methyl hex-3-enoate, also known as methyl (3E)-hex-3-enoate, is an organic compound that is prepared by selective hydrogenation of methyl sorbate. It is a clear colorless to faintly yellow liquid with a sweet, green, banana-like, slightly acidic taste, and fruity nuances of pineapple, pear, apple, and passion fruit.
Uses
Used in Flavor Industry:
Methyl hex-3-enoate is used as a flavoring agent for its sweet, sharp green, juicy fresh fruity aroma with tropical and vegetative nuances. It is particularly suitable for enhancing the taste and aroma of various food products.
Used in Fragrance Industry:
Methyl hex-3-enoate is used as a fragrance ingredient for its sweet, fruity, and slightly acidic scent. It can be used in the formulation of perfumes, colognes, and other personal care products to provide a pleasant and refreshing aroma.
Used in Chemical Synthesis:
Methyl hex-3-enoate can be used as a building block in the synthesis of various chemicals and compounds. Its unique chemical structure makes it a valuable intermediate in the production of other organic compounds.
Used in Research and Development:
Methyl hex-3-enoate is used in research and development for studying its chemical properties, reactivity, and potential applications in various fields, including pharmaceuticals, materials science, and biotechnology.
Synthesis Reference(s)
Chemistry Letters, 11, p. 715, 1982The Journal of Organic Chemistry, 51, p. 537, 1986 DOI: 10.1021/jo00354a027
Check Digit Verification of cas no
The CAS Registry Mumber 2396-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,9 and 6 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 2396-78:
(6*2)+(5*3)+(4*9)+(3*6)+(2*7)+(1*8)=103
103 % 10 = 3
So 2396-78-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H12O2/c1-3-4-5-6-7(8)9-2/h4-5H,3,6H2,1-2H3
2396-78-3Relevant articles and documents
Catalytic Regio- and Enantioselective Oxytrifluoromethylthiolation of Aliphatic Internal Alkenes by Neighboring Group Assistance
Xu, Jia,Zhang, Yuanyuan,Qin, Tian,Zhao, Xiaodan
supporting information, p. 6384 - 6388 (2018/10/09)
Chiral selenide-catalyzed oxytrifluoromethylthiolation of aliphatic internal alkenes by a formally intermolecular strategy is disclosed, affording CF3S 1,3-amino alcohol and 1,3-diol derivatives with high regio-, enantio-, and diastereoselectivities. The reactions are promoted by a neighboring imide or ester group on substrates via a six-membered ring transition state. This assistance strategy is also successfully applied to the regio- and diastereoselective oxyhalofunctionalization of internal alkenes and the conversion of alkynes.
