19355-58-9 Usage
Uses
Used in Fragrance Industry:
Dehydrololiolide is used as a scent enhancer for its characteristic odor, adding depth and complexity to fragrances.
Used in Cosmetic Industry:
In the cosmetic industry, dehydrololiolide is utilized as a fragrance ingredient, enhancing the sensory experience of cosmetic products.
Used in Pharmaceutical Industry:
Dehydrololiolide is used as a potential therapeutic agent due to its anti-inflammatory and antioxidant properties, which may contribute to the treatment of various health conditions.
Used in Healthcare:
Its anti-cancer and anti-microbial effects position dehydrololiolide as a candidate for further research and development in healthcare, particularly for the prevention and treatment of certain diseases.
Used in Research:
Dehydrololiolide's diverse biological activities make it a valuable subject for scientific research, exploring its potential in new therapeutic applications and understanding its mechanisms of action.
Check Digit Verification of cas no
The CAS Registry Mumber 19355-58-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,3,5 and 5 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19355-58:
(7*1)+(6*9)+(5*3)+(4*5)+(3*5)+(2*5)+(1*8)=129
129 % 10 = 9
So 19355-58-9 is a valid CAS Registry Number.
19355-58-9Relevant academic research and scientific papers
Simple Synthesis of Dehydrololiolide
Tamura, Hiroshi,Fujita, Akira,Takagi, Yoshikazu,Kitahara, Takeshi,Mori, Kenji
, p. 1902 - 1903 (2007/10/02)
Dehydrololiolide, isolated from tobacco leaves, was synthesized via the intramolecular alsol reaction, Reformatsky reaction, and Wittig reaction of the key intermediate keto esters.
NEW SYNTHESIS OF LOLIOLIDE, DEHYDROLOLIOLIDE, AND 3-OXOACTINIDOL
Takazawa, Osamu,Kogami, Kunio,Hayashi, Kazuo
, p. 63 - 64 (2007/10/02)
Loliolide, dehydrololiolide, and 3-oxoactinidol were synthesized from megastigma-4,6,8-trien-3-one by regioselective ozonolysis and epoxidation.
