53398-80-4 Usage
Description
PROPIONIC ACID TRANS-2-HEXEN-1-YL ESTER, also known as (E)-2-Hexenyl propionate, is the propanoate ester of (2E)-hex-2-en-1-ol. It is characterized by its green, oily fruity taste with a slight soapy mouthfeel and a fruity odor with a ripe apple/pear note.
Uses
Used in Flavor and Fragrance Industry:
PROPIONIC ACID TRANS-2-HEXEN-1-YL ESTER is used as a flavoring agent for its green, fruity apple and pear pulp taste with creamy and powdery nuances. It is particularly suitable for enhancing the flavor of food products that aim to mimic the taste of fresh fruits.
Used in Perfumery:
PROPIONIC ACID TRANS-2-HEXEN-1-YL ESTER is used as a fragrance ingredient for its fruity odor with a ripe apple/pear note, adding a fresh and natural scent to perfumes and other scented products.
Used in the Food Industry:
PROPIONIC ACID TRANS-2-HEXEN-1-YL ESTER is used as an additive in the food industry to provide a green, oily fruity taste and a slight soapy mouthfeel, which can be beneficial in creating or enhancing the flavor profiles of various food products, especially those with fruit-based flavors.
Used in the Beverage Industry:
PROPIONIC ACID TRANS-2-HEXEN-1-YL ESTER is used as a flavor enhancer in the beverage industry, particularly for drinks that aim to capture the essence of green, fruity apple and pear flavors, providing a refreshing and natural taste experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 53398-80-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53398-80:
(7*5)+(6*3)+(5*3)+(4*9)+(3*8)+(2*8)+(1*0)=144
144 % 10 = 4
So 53398-80-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H16O2/c1-3-5-6-7-8-11-9(10)4-2/h6-7H,3-5,8H2,1-2H3/b7-6-
53398-80-4Relevant articles and documents
Copper Hydride Catalyzed Reductive Claisen Rearrangements
Wong, Kong Ching,Ng, Elvis,Wong, Wing-Tak,Chiu, Pauline
, p. 3709 - 3712 (2016/03/08)
An efficient reductive Claisen rearrangement, catalyzed by in situ generated copper hydride and stoichiometric in diethoxymethylsilane, has been developed. Yields of up to 95 ;% with good to excellent diastereoselectivities were observed in this reaction. Mechanistic studies showed that the stereospecific rearrangement proceeded via a chair transition state of (E)-silyl ketene acetals as intermediates and not via the copper enolates.