33081-34-4 Usage
Description
(βS,2S,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2α-ethanol is a complex organic compound characterized by a tetrahydrofuran ring with a vinyl group and two methyl groups attached. It also features an alcohol functional group connected to the tetrahydrofuran ring. The stereochemistry of this compound is defined by the βS, 2S, and 5S configurations, which describe the arrangement of the substituents around the tetrahydrofuran ring. This unique structure and the presence of various functional groups suggest potential applications in fields such as organic synthesis, medicinal chemistry, and materials science.
Uses
Used in Organic Synthesis:
(βS,2S,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2α-ethanol is used as an intermediate in organic synthesis for the creation of more complex molecules. Its unique structure and functional groups make it a valuable building block for the development of novel compounds with specific properties.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (βS,2S,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2α-ethanol may be utilized as a precursor for the synthesis of bioactive molecules. Its structural features could be exploited to design new pharmaceuticals with potential therapeutic applications.
Used in Materials Science:
(βS,2S,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2α-ethanol could also be employed in materials science as a component in the development of new materials with specific characteristics. Its tetrahydrofuran ring and functional groups may contribute to the creation of materials with unique mechanical, electrical, or optical properties.
Used in Fragrance Industry:
(βS,2S,5S)-β,5-Dimethyl-5β-vinyltetrahydrofuran-2α-ethanol may be used as a component in the fragrance industry to create unique scents. Its complex structure and functional groups could contribute to the development of novel fragrances with distinct olfactory profiles.
Used in Flavor Industry:
Similarly, in the flavor industry, this compound could be used to develop new taste profiles for the food and beverage sector. Its unique structure may allow for the creation of innovative flavors that could enhance the sensory experience of consumers.
Check Digit Verification of cas no
The CAS Registry Mumber 33081-34-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,8 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33081-34:
(7*3)+(6*3)+(5*0)+(4*8)+(3*1)+(2*3)+(1*4)=84
84 % 10 = 4
So 33081-34-4 is a valid CAS Registry Number.
33081-34-4Relevant articles and documents
INTRAMOLECULAR REACTIONS OF ALLYLOXY RADICALS
Johns, Amanda,Murphy, John A.,Sherburn, Michael S.
, p. 7835 - 7858 (2007/10/02)
Allyloxy radicals formed by epoxide cleavage, have cyclised onto appropriately positioned alkenes to form tetrahydrofurans, and the diastereoselectivity of the cyclisation has been studied.The reaction was used to synthesise lilac alcohols which were then used to confirm the stereochemistry of such cyclisations.
A HIGHLY STEREOSELECTIVE SYNTHESIS OF DAVANONE
Bartlett, Paul A.,Holmes, Christopher P.
, p. 1365 - 1368 (2007/10/02)
Iodocyclization of the anti 4-bromobenzyl ether acetate 4f is a key step in the first stereocontrolled synthesis of the trisubstituted tetrahydrofuran davanone.
