80736-91-0 Usage
Description
(4S)-3,4-dihydroxy-2,6,6-trimethylcyclohex-2-en-1-one, also known as carvone, is a naturally occurring compound found in a variety of essential oils, such as spearmint and caraway. It is characterized by its pleasant minty and slightly spicy aroma, making it a popular choice for use as a flavoring agent in the food and beverage industry. Beyond its sensory appeal, carvone also exhibits potential medicinal properties, including anti-inflammatory, antispasmodic, and antimicrobial effects, which contribute to its diverse applications across different sectors.
Uses
Used in Flavor and Fragrance Industry:
Carvone is used as a flavoring agent for its characteristic minty and slightly spicy aroma, adding a unique taste to various foods and beverages.
Used in Personal Care Products:
Carvone is utilized in the formulation of fragrances and personal care products due to its pleasant scent, enhancing the sensory experience for consumers.
Used as a Potential Insect Repellent:
(4S)-3,4-dihydroxy-2,6,6-trimethylcyclohex-2-en-1-one has been studied for its potential as an insect repellent, offering a natural alternative to chemical-based repellents.
Used in Medicinal Applications:
Carvone is explored for its potential medicinal properties, such as anti-inflammatory, antispasmodic, and antimicrobial effects, which could contribute to the development of new treatments for various health conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 80736-91-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,3 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80736-91:
(7*8)+(6*0)+(5*7)+(4*3)+(3*6)+(2*9)+(1*1)=140
140 % 10 = 0
So 80736-91-0 is a valid CAS Registry Number.
80736-91-0Relevant articles and documents
PROCESS FOR PREPARING (4S)- OR (4R)-3,4-DIHYDROXY-2,6,6-TRIMETHYLCYCLOHEX-2-ENONE
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Page/Page column 16; 17, (2018/07/29)
The present invention relates to a new process for the preparation of one of the enantiomers of 3,4-dihydroxy-2,6,6-trimethylcyclohex-2-enoneand to a process for preparing (3S,3'S)-astaxanthin, which comprises the step of providing the (4S)-enantiomerof 3
Technische Verfahren zur Synthese von Carotinoiden und verwandten Verbindungen aus 6-Oxo-isophoron. III. Ein neues Konzept fuer die Synthese der enantiomeren Astaxanthine
Zell, Reinhard,Widmer, Erich,Lukac, Teodor,Leuenberger, Hans Georg Wilhelm,Schoenholzer, Peter,Broger, Emil A.
, p. 2447 - 2462 (2007/10/02)
A new and efficient concept for the total synthesis of (3S,3'S)- and (3R,3'R)-astaxanthin (1a and 1c, resp.) in high overall yield and up to 99,2percent enantiomeric purity is described.Key intermediates are the (S)- and (R)-acetals 10 and 17, respectively (Scheme 2).These chiral building blocks were synthesized via three different routes: a) functionalization of enantiomeric 3-hydroxy-6-oxo-isophorons 2 and 11, respectively (Scheme 2); b) optical resolution of 3,4-dihydroxy-compound 19 (Scheme 3), and c) fermentative reductions of 6-oxo-isophorone derivatives (Schemes 4 and 5). - The absolute configurations of the two intermediates 12 and 13 (Scheme 2) have been confirmed by X-ray analysis.The final steps leading to the enantiomeric astaxanthins are identical with those described for optically inactive astaxanthin .
