20895-16-3 Usage
Uses
Used in Food Industry:
1-(2-furyl)-3-methyl-butan-1-one is used as a flavoring agent for its sweet, caramel-like aroma and flavor, which enhances the taste and aroma of various food products, particularly those derived from fruits and vegetables.
Used in Coffee Industry:
In the coffee industry, 1-(2-furyl)-3-methyl-butan-1-one is used as an aroma component to improve the overall sensory experience of roasted coffee, contributing to its distinct and appealing scent.
Used in Health and Wellness Applications:
Furaneol is also utilized in the health and wellness sector due to its potential antioxidant and anti-inflammatory properties, which may offer various health benefits when consumed in small amounts.
Used as a Food Additive:
1-(2-furyl)-3-methyl-butan-1-one is used as a safe additive in the food industry, where it is added in small quantities to improve the taste and aroma of a wide range of products.
Check Digit Verification of cas no
The CAS Registry Mumber 20895-16-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 20895-16:
(7*2)+(6*0)+(5*8)+(4*9)+(3*5)+(2*1)+(1*6)=113
113 % 10 = 3
So 20895-16-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H12O2/c1-7(2)6-8(10)9-4-3-5-11-9/h3-5,7H,6H2,1-2H3
20895-16-3Relevant academic research and scientific papers
C5′-alkyl substitution effects on digitoxigenin α-l-glycoside cancer cytotoxicity
Wang, Hua-Yu Leo,Wu, Bulan,Zhang, Qi,Kang, Sang-Woo,Rojanasakul, Yon,O'Doherty, George A.
scheme or table, p. 259 - 263 (2011/06/16)
A highly regio- and stereoselective asymmetric synthesis of various C5′-alkyl side chains of rhamnosyl- and amicetosyl-digitoxigenin analogues has been established via palladium-catalyzed glycosylation with postglycosylated dihydroxylation or diimide reduction. The C5′-methyl group in both α-l-rhamnose and α-l-amicetose digitoxin analogues displayed a steric directed apoptosis induction and tumor growth inhibition against nonsmall cell human lung cancer cells (NCI-H460). The antitumor activity is significantly reduced when the steric hindrance is increased at the C5′-stereocenter.
