68017-33-4 Usage
Uses
Used in Fragrance Industry:
5-Methyl-5-hexen-3-yn-2-ol is used as a fragrance ingredient in perfumes and cosmetics for its pleasant and fresh aroma, enhancing the sensory experience of these products.
Used in Pharmaceutical Industry:
5-Methyl-5-hexen-3-yn-2-ol is used as a precursor or intermediate in the synthesis of various compounds within the pharmaceutical industry, leveraging its unique chemical structure to create new medicinal agents.
Used in Agrochemical Industry:
In the agrochemical sector, 5-Methyl-5-hexen-3-yn-2-ol serves as a precursor or intermediate in the development of agrochemicals, potentially contributing to the creation of new products for agricultural applications.
Organic Synthesis and Chemical Research:
5-Methyl-5-hexen-3-yn-2-ol is utilized in organic synthesis and chemical research due to its intriguing molecular structure, which includes a hexenyl group and an alkyne group, offering opportunities for the development of novel chemical reactions and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 68017-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,1 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 68017-33:
(7*6)+(6*8)+(5*0)+(4*1)+(3*7)+(2*3)+(1*3)=124
124 % 10 = 4
So 68017-33-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H10O/c1-6(2)4-5-7(3)8/h7-8H,1H2,2-3H3
68017-33-4Relevant academic research and scientific papers
The Intramolecular Enyne Diels-Alder Reaction. Stereoselective Construction of Tricyclic Dioxadienones and Mechanistic Outline
Hoffmann, H. M. R.,Krumwiede, D.,Mucha, B.,Oehlerking, H. H.,Prahst, G. W.
, p. 8999 - 9018 (2007/10/02)
4-Methylpent-4-en-2-yn-1-ols and 6-hydroxy-2,3-dihydro-6H-pyran-3-ones are condensed in different ways to a series of tricyclic dioxadienones which contain the basic framework of the cadlinolides A mechanism of the intramolecular enyne-ene cycloisomerization and the origin of the resulting type I and type II dienes is proposed.
