13678-60-9 Usage
Description
FEMA 3283, also known as Furfuryl isovalerate, is a synthetic compound derived from the esterification of furfuryl alcohol with isovaleric chloride. It is characterized by its distinct berry, fruity, and ripe aroma, making it a popular choice in the flavor and fragrance industry.
Uses
Used in Flavor Industry:
FEMA 3283 is used as a flavoring agent for its characteristic berry, fruity, and ripe aroma. It is commonly utilized in the creation of various food and beverage products to enhance their taste and provide a pleasant sensory experience for consumers.
Used in Fragrance Industry:
FEMA 3283 is also used as a fragrance ingredient due to its appealing scent. It can be found in a wide range of personal care and cosmetic products, such as perfumes, colognes, and body care items, to add a unique and attractive fragrance.
Preparation
By esterifcation of furfuryl alcohol with isovaleric chloride.
Check Digit Verification of cas no
The CAS Registry Mumber 13678-60-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,6,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 13678-60:
(7*1)+(6*3)+(5*6)+(4*7)+(3*8)+(2*6)+(1*0)=119
119 % 10 = 9
So 13678-60-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H14O3/c1-8(2)6-10(11)13-7-9-4-3-5-12-9/h3-5,8H,6-7H2,1-2H3
13678-60-9Relevant articles and documents
HMF and furfural: Promising platform molecules in rhodium-catalyzed carbonylation reactions for the synthesis of furfuryl esters and tertiary amides
Qi, Xinxin,Zhou, Rong,Ai, Han-Jun,Wu, Xiao-Feng
, p. 215 - 221 (2019/11/25)
A biomass involved rhodium-catalyzed carbonylative synthesis of furfuryl esters and tertiary amides has been developed. 5-Hydroxymethylfurfural (HMF) was used as both substrate and CO surrogate for the first time in a carbonylation reaction, and both alkyl and aryl iodides were tolerated well to afford the desired furfuryl esters in moderate to good yields. In addition, furfural was also utilized as a CO source for the synthesis of tertiary amides. A variety of tertiary amides were obtained in moderate to excellent yields with good functional groups compatibility. Notably, tertiary amines were used as the amine source through a C[sbnd]N bond cleavage pathway in the absence of additional oxidant.
