77722-56-6 Usage
Tertiary alcohol
It is classified as a tertiary alcohol This means that the hydroxyl (OH) group is attached to a carbon atom that is itself bonded to two other carbon atoms, giving it a specific chemical reactivity and properties.
Fruity and floral aroma
It is commonly used as a flavoring agent in the food industry 2,5-dimethylhex-1-en-3-ol imparts a pleasant fruity and floral aroma to various food products, making it a popular choice for flavor enhancement.
Production of perfumes and fragrances
The compound is also used in the production of perfumes and fragrances Due to its appealing scent, 2,5-dimethylhex-1-en-3-ol is a valuable ingredient in creating various personal care and household products.
Potential pharmaceutical and cosmetic applications
2,5-dimethylhex-1-en-3-ol has potential applications in the pharmaceutical and cosmetic industries Its pleasant scent and chemical properties make it a candidate for use in various products, such as medications and skincare items.
Health risks
The compound should be handled with care as it may pose health risks if not used properly Due to its chemical nature, 2,5-dimethylhex-1-en-3-ol may have potential adverse effects on human health if not used according to recommended guidelines and safety precautions.
Check Digit Verification of cas no
The CAS Registry Mumber 77722-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,7,2 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 77722-56:
(7*7)+(6*7)+(5*7)+(4*2)+(3*2)+(2*5)+(1*6)=156
156 % 10 = 6
So 77722-56-6 is a valid CAS Registry Number.
77722-56-6Relevant articles and documents
Palladium-catalyzed intramolecular reductive olefin hydrocarbonation: Benzylic hydrogen serving as a new hydrogen donor
Dong, Xu,Cui, Jie,Song, Jian,Han, Ying,Liu, Qing,Dong, Yunhui,Liu, Hui
supporting information, p. 4903 - 4906 (2017/07/11)
A palladium-catalyzed intramolecular hydrocarbonation of unactivated alkenes was achieved, in which toluene is used as a hydrogen donor for the first time. The radical transfer hydrogenation is designed and realized based on the Bond Dissociation Energy (
SYNTHESIS AND SOME REACTIONS OF ISOPROPENYLOXIRANE
Gevorkyan, A. A.,Kazaryan, P. I.,Avakyan, S. V.
, p. 372 - 378 (2007/10/02)
A convenient method for the synthesis of isopropenyloxirane by dehydrohalogenation of halohydrins obtained by isomerization of 1-halo-3-methyl-2,3-epoxybutanes was developed.The reactions of isopropenyloxirane with alcohols, water, secondary amines, hydrogen halides, dichlorocarbene, acetic acid anhydrides, and Grignard reagents were studied.
