18521-06-7 Usage
Description
(3E)-2-methyloct-3-en-2-ol, also known as 2-methyloct-3-en-2-ol, is a chemical compound with the molecular formula C9H18O. It is an alcohol derivative with a double bond at the third carbon and a hydroxyl group attached to the second carbon in the chain. (3E)-2-methyloct-3-en-2-ol is commonly found in essential oils and is characterized by its slightly floral and fruity scent.
Uses
Used in Fragrance and Flavor Industry:
(3E)-2-methyloct-3-en-2-ol is used as a natural aroma compound for adding a fresh and sweet scent to various products such as perfumes, lotions, and household cleaners. Its natural and pleasant aroma makes it a valuable ingredient in creating appealing fragrances for consumer products.
Used in Pharmaceutical Industry:
(3E)-2-methyloct-3-en-2-ol is studied for its potential antibacterial and antiviral properties, which makes it a valuable ingredient in the development of pharmaceutical products. Its ability to combat bacteria and viruses contributes to the creation of effective treatments and preventive measures against infections.
Used in Cosmetic Industry:
In the cosmetic industry, (3E)-2-methyloct-3-en-2-ol is utilized for its beneficial properties, including its potential antibacterial and antiviral actions. This makes it suitable for inclusion in skincare and beauty products, where it can contribute to maintaining healthy and clean skin while also providing a pleasant scent.
Check Digit Verification of cas no
The CAS Registry Mumber 18521-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,5,2 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 18521-06:
(7*1)+(6*8)+(5*5)+(4*2)+(3*1)+(2*0)+(1*6)=97
97 % 10 = 7
So 18521-06-7 is a valid CAS Registry Number.
18521-06-7Relevant articles and documents
On the mechanism of the copper-catalyzed enantioselective 1,4-addition of Grignard reagents to α,β-unsaturated carbonyl compounds
Harutyunyan, Syuzanna R.,Lopez, Fernando,Browne, Wesley R.,Correa, Arkaitz,Pena, Diego,Badorrey, Ramon,Meetsma, Auke,Minnaard, Adriaan J.,Feringa, Ben L.
, p. 9103 - 9118 (2006)
The mechanism of the enantioselective 1,4-addition of Grignard reagents to α,β-unsaturated carbonyl compounds promoted by copper complexes of chiral ferrocenyl diphosphines is explored through kinetic, spectroscopic, and electrochemical analysis. On the basis of these studies, a structure of the active catalyst is proposed. The roles of the solvent, copper halide, and the Grignard reagent have been examined. Kinetic studies support a reductive elimination as the rate-limiting step in which the chiral catalyst, the substrate, and the Grignard reagent are involved. The thermodynamic activation parameters were determined from the temperature dependence of the reaction rate. The putative active species and the catalytic cycle of the reaction are discussed.
