60159-70-8 Usage
Description
1-(2-ethoxyphenyl)butane-1,3-dione, also known as ethyl 2,2-diphenylbutanoate, is a chemical compound with the molecular formula C13H18O3. It is a colorless to pale yellow liquid with a sweet, fruity, and floral odor. 1-(2-ethoxyphenyl)butane-1,3-dione is known for its low volatility and relative stability under normal conditions.
Uses
Used in Fragrance and Flavor Industry:
1-(2-ethoxyphenyl)butane-1,3-dione is used as a fragrance compound for its sweet, fruity, and floral scent. It is added to various personal care and household products to enhance their aroma, providing a pleasant and appealing scent to consumers.
Used in Food Industry:
In the food industry, 1-(2-ethoxyphenyl)butane-1,3-dione is used as a flavoring agent. Its unique and desirable odor characteristics make it a valuable addition to the flavor profiles of various food products, contributing to a more enjoyable and memorable taste experience for consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 60159-70-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,1,5 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 60159-70:
(7*6)+(6*0)+(5*1)+(4*5)+(3*9)+(2*7)+(1*0)=108
108 % 10 = 8
So 60159-70-8 is a valid CAS Registry Number.
60159-70-8Relevant articles and documents
A General Proline-Catalyzed Synthesis of 4,5-Disubstituted N-Sulfonyl-1,2,3-Triazoles from 1,3-Dicarbonyl Compounds and Sulfonyl Azide
Rajasekar, Shanmugam,Anbarasan, Pazhamalai
, p. 4563 - 4567 (2019)
An efficient proline-catalyzed synthesis of 4,5-disubstituted-N-sulfonyl-1,2,3-triazoles has been accomplished from 1,3-dicarbonyl compounds and sulfonyl azides. The developed reaction is suitable for various symmetrical and unsymmetrical 1,3-dicarbonyl compounds, tolerates various functional groups and affords 4,5-disubstituted-N-sulfonyl-1,2,3-triazoles in good yield with excellent regioselectivity. Rhodium-catalyzed denitrogenative functionalization of 4,5-disubstituted-N-sulfonyl-1,2,3-triazoles further demonstrates their utility in organic synthesis.
