60894-97-5 Usage
Description
(4R)-2-methyl-6-methylideneocta-2,7-dien-4-ol, also known as R-Ipsdienol, is an isomer of S-Ipsdienol, a terpene compound. It is characterized by its unique molecular structure, which includes a methyl group at the 2nd position, a methylene group at the 6th position, and a hydroxyl group at the 4th position. (4R)-2-methyl-6-methylideneocta-2,7-dien-4-ol is derived from natural sources and exhibits various properties that make it suitable for a range of applications.
Uses
Used in Food Industry:
(4R)-2-methyl-6-methylideneocta-2,7-dien-4-ol is used as an antioxidant and antimicrobial agent in the food industry. Its ability to prevent oxidation and inhibit the growth of microorganisms helps to extend the shelf life of various food products, ensuring their freshness and safety for consumption.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (4R)-2-methyl-6-methylideneocta-2,7-dien-4-ol is utilized for its potential therapeutic properties. Its antioxidant and antimicrobial characteristics can be harnessed in the development of new drugs or formulations, targeting a variety of health conditions.
Used in Pesticide Industry:
(4R)-2-methyl-6-methylideneocta-2,7-dien-4-ol is also used in the pesticide industry, where it serves as a conspecific aggregation pheromone for the Asian larch bark beetle, Ips subelongatus. By mimicking the natural pheromones of these insects, it can be employed as a part of integrated pest management strategies to control their populations and reduce the damage they cause to trees and forests.
Check Digit Verification of cas no
The CAS Registry Mumber 60894-97-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,8,9 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 60894-97:
(7*6)+(6*0)+(5*8)+(4*9)+(3*4)+(2*9)+(1*7)=155
155 % 10 = 5
So 60894-97-5 is a valid CAS Registry Number.
60894-97-5Relevant articles and documents
Enantioselective Isoprenylboration Reaction of Aldehydes Catalyzed by a Chiral Phosphoric Acid
Zhang, Yu-Long,He, Bo-Jun,Xie, Yi-Wen,Wang, Yu-Hao,Wang, Yi-Long,Shen, Yong-Cun,Huang, Yi-Yong
supporting information, p. 3074 - 3079 (2019/05/15)
The BINOL-derived chiral phosphoric acid (R)-TRIP is utilized as an organocatalyst in the asymmetric isoprenylboration reaction of aldehydes, wherein hydrogen-bond interactions play a key role in the control of enantioselectivity. A wide arrays of enantioenriched dienyl homoallyl alcohols, including two natural products (?)-Ipsdienol and (?)-Ipsenol, have been successfully constituted. The synthetic application to chiral isoprenylated isobenzofuranone, vinyloxirane and cyclohexene derivatives has also been disclosed. (Figure presented.).
Catalytic asymmetric allylic transfer reactions for the Enantioselective synthesis of dienyl and enynyl alcohols
Yu, Chan-Mo,Jeon, Miyoo,Lee, Jae-Young,Jeon, Junha
, p. 1143 - 1148 (2007/10/03)
Efficient catalytic asymmetric allylic transfer reactions of achiral aldehydes with 2-ethynyl- and 2-ethenyl-2-propenyl-stannane promoted by BINOL-TiIV complex with synergetic reagent are achieved for the synthesis of homoenynyl- and dienyl alcohols with high levels of enantioselectivity. The range of enantioselectivity is 84-99% ee with good chemical yields. The application of catalytic asymmetric dienylation in a single operation was exemplified by the enantioselective synthesis of naturally occurring (-)-Ipsdienol and (-)-Ipsenol.
ENANTIOMERIC PAIRS OF IPSENOL AND IPSDIENOL USING ASYMMETRIC ISOPRENYLBORYLATION
Bubnov, Yu. N.,Etinger, M. Yu.
, p. 1502 (2007/10/02)
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