73455-01-3 Usage
Description
1-(1,3-Benzodioxol-5-yl)propyl acetate, commonly known as safrole acetate, is a chemical compound with the molecular formula C12H14O4. It is derived from the essential oil of sassafras and other plants, and is characterized by its clear, colorless liquid appearance and sweet, floral odor.
Uses
Used in Fragrance Industry:
1-(1,3-Benzodioxol-5-yl)propyl acetate is used as a fragrance ingredient for its sweet, floral scent. It is widely utilized in the production of perfumes and cosmetic products to provide a pleasant and long-lasting aroma.
Used in Flavor and Food Industry:
Safrole acetate is also used as a flavoring agent in the food and beverage industry. Its unique flavor profile adds a distinct taste to various products, enhancing their overall sensory experience.
Used in Pharmaceutical Industry:
1-(1,3-Benzodioxol-5-yl)propyl acetate has been studied for its potential medicinal properties, including antimicrobial and antioxidant effects. While its use in this industry is still under investigation, it shows promise for future applications in the development of new drugs and treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 73455-01-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,4,5 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 73455-01:
(7*7)+(6*3)+(5*4)+(4*5)+(3*5)+(2*0)+(1*1)=123
123 % 10 = 3
So 73455-01-3 is a valid CAS Registry Number.
73455-01-3Relevant articles and documents
DDQ catalyzed benzylic acetoxylation of arylalkanes: a case of exquisitely controlled oxidation under sonochemical activation
Kumar, Vinod,Sharma, Abhishek,Sharma, Meenakshi,Sharma, Upendra K.,Sinha, Arun K.
, p. 9718 - 9723 (2008/02/12)
Acetoxylated arylalkanes are selectively obtained via sonochemical activation of DDQ catalyzed benzylic oxidation of arylalkanes in the presence of anhydrous acetic acid. The method gives an exquisite control of benzylic acetoxylation under ultrasound, in contrast to the uncontrolled oxidation observed under conventional heating or microwave activation. In addition, the developed method could be?a useful strategy for the synthesis of industrially important enantiopure benzyl alcohols due to the easy amenability of obtained acetoxylated products toward chiral resolution.
