97232-74-1 Usage
Description
(E,E,E,E,E,E)-(1)-2,6,10,15,19,23-Hexamethyltetracosa-1,6,10,14,18,22-hexaen-3-ol is a naturally occurring terpenoid alcohol with a complex structure, featuring six double bonds and a long hydrocarbon chain. It is found in various plant species and is known for its potential antimicrobial, anti-inflammatory, and antioxidant properties, making it a versatile compound with applications in different industries.
Uses
Used in Cosmetics and Personal Care Products:
(E,E,E,E,E,E)-(1)-2,6,10,15,19,23-Hexamethyltetracosa-1,6,10,14,18,22-hexaen-3-ol is used as a fragrance ingredient in the cosmetics and personal care industry due to its pleasant scent and natural origin.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (E,E,E,E,E,E)-(1)-2,6,10,15,19,23-Hexamethyltetracosa-1,6,10,14,18,22-hexaen-3-ol is studied for its potential antimicrobial, anti-inflammatory, and antioxidant properties, making it a promising candidate for the development of new drugs and treatments.
Used in Medical Research:
(E,E,E,E,E,E)-(1)-2,6,10,15,19,23-Hexamethyltetracosa-1,6,10,14,18,22-hexaen-3-ol is also of interest in medical research due to its potential therapeutic applications, including its antimicrobial, anti-inflammatory, and antioxidant properties, which could contribute to the development of novel medical treatments and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 97232-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,2,3 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 97232-74:
(7*9)+(6*7)+(5*2)+(4*3)+(3*2)+(2*7)+(1*4)=151
151 % 10 = 1
So 97232-74-1 is a valid CAS Registry Number.
97232-74-1Relevant articles and documents
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Yasuda,A. et al.
, p. 1705 - 1708 (1979)
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Yasuda,A. et al.
, p. 6513 - 6514 (1974)
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Solid-phase selenium-catalyzed selective allylic chlorination of polyprenoids: Facile syntheses of biologically active terpenoids
Barrero, Alejandro F.,Del Moral, Jose F. Quilez,Herrador, M. Mar,Cortes, Manuel,Arteaga, Pilar,Catalan, Julieta V.,Sanchez, Elena M.,Arteaga, Jesus F.
, p. 5811 - 5814 (2007/10/03)
Regioselective halogenation of the terminal isopropylidene unit of different acyclic polyolefinic polyprenoids (farnesyl acetate, geranylgeranyl acetate, squalene, etc.) using NCS/catalytic polymer-supported selenenyl bromide is described; good to excellent yields are obtained (68-96%). The first applications of this protocol include the concise synthesis of bioactive terpenoids 1-3.
Trisnorsqualene Alcohol, a Potent Inhibitor of Vertebrate Squalene Epoxidase
Sen, Stephanie E.,Prestwich, Glenn D.
, p. 1508 - 1510 (2007/10/02)
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