27185-77-9 Usage
Uses
Used in Fragrance Industry:
2,4,4-trimethyl-3-(3-oxo-1-butenyl)cyclohex-2-en-1-one is used as a fragrance ingredient for its sweet, floral scent, contributing to the overall aroma profile of perfumes, soaps, detergents, and cosmetics.
Used in Flavoring Industry:
In the flavoring industry, 2,4,4-trimethyl-3-(3-oxo-1-butenyl)cyclohex-2-en-1-one is used as a flavoring agent to enhance the taste and aroma of various food and beverage products.
Used in Household Products:
2,4,4-trimethyl-3-(3-oxo-1-butenyl)cyclohex-2-en-1-one is used as an odor agent in air fresheners and other household products to provide a pleasant and long-lasting scent.
Used in Pest Control Products:
In the pest control industry, 2,4,4-trimethyl-3-(3-oxo-1-butenyl)cyclohex-2-en-1-one is used as an insecticidal and bactericidal additive, leveraging its natural properties to control and eliminate pests effectively.
Check Digit Verification of cas no
The CAS Registry Mumber 27185-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,1,8 and 5 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27185-77:
(7*2)+(6*7)+(5*1)+(4*8)+(3*5)+(2*7)+(1*7)=129
129 % 10 = 9
So 27185-77-9 is a valid CAS Registry Number.
InChI:InChI=1/C13H18O2/c1-9(14)5-6-11-10(2)12(15)7-8-13(11,3)4/h5-6H,7-8H2,1-4H3
27185-77-9Relevant academic research and scientific papers
DBU/O2-Mediated Oxidation of Dienones
Athawale, Paresh R.,Kalmode, Hanuman P.,Reddy, D. Srinivasa
, p. 9200 - 9205 (2021/07/19)
Herein, we describe a DBU/O2-promoted novel method for oxidation of dienones to 2,6-dione derivatives. The reaction involves treatment of a dienone with DBU in acetonitrile employing molecular oxygen as the oxidant. Metal free conditions and an eco-friendly reagent are the striking features of this protocol. This transformation proceeds through a peroxide intermediate that upon Kornblum-DeLaMare rearrangement produces 2,6-diones. The method was successfully utilized for the synthesis of (±)-pleodendione with improved yields versus those of the traditional PDC-TBHP method.
