115-71-9 Usage
Description
5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer is a complex organic compound with a unique molecular structure. It is characterized by its tricyclic core and multiple methyl groups, which contribute to its distinct chemical properties and potential applications.
Uses
Used in Perfumes, Soaps, and Detergents:
5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer is used as a fragrance ingredient in the perfume industry, providing a unique and pleasant scent to various products. Its incorporation in soaps and detergents not only enhances the sensory experience but also contributes to the overall effectiveness of these products.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, 5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer may be utilized for its potential therapeutic properties. Its unique molecular structure could be harnessed to develop new drugs or improve the delivery and efficacy of existing medications.
Used in Cosmetics:
The stereoisomer may also find applications in the cosmetics industry, where it could be used as an active ingredient in skincare and beauty products. Its potential benefits may include moisturizing, anti-aging, or protective properties, depending on its specific characteristics and interactions with other components.
Used in Aromatherapy:
5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer could be employed in aromatherapy practices, where its unique scent and potential therapeutic properties may contribute to relaxation, stress relief, or other wellness benefits.
Used in Flavor Industry:
In the flavor industry, the stereoisomer may be used to enhance the taste and aroma of various food and beverage products. Its unique molecular structure could provide a distinct flavor profile, adding depth and complexity to the final product.
Used in Research and Development:
Due to its complex structure and potential applications, 5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer may be valuable in research and development efforts. Scientists and chemists could use this compound to study its properties, explore new applications, or develop innovative products across various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 115-71-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,1 and 5 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 115-71:
(5*1)+(4*1)+(3*5)+(2*7)+(1*1)=39
39 % 10 = 9
So 115-71-9 is a valid CAS Registry Number.
InChI:InChI=1/C15H24O/c1-10(9-16)5-4-6-14(2)11-7-12-13(8-11)15(12,14)3/h5,11-13,16H,4,6-9H2,1-3H3/b10-5-/t11?,12?,13?,14-,15?/m0/s1
115-71-9Relevant articles and documents
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Corey,E.J. et al.
, p. 6314 - 6319 (1970)
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A STEREOSELECTIVE SYNTHESIS OF β,γ-DISUBSTITUTED ALLYLIC ALCOHOLS OF Z-CONFIGURATION
Tamura, Mitsuhisa,Suzukamo, Gohu
, p. 577 - 580 (2007/10/02)
Reaction of alkyllithiums 1 with isoprene epoxide 2 gives β,γ-disubstituted allylic alcohols 3 of Z-configuration.The reaction of ?-lithiotricyclene as alkyllithium gives α-santalol 5, which is one of the main constituents in East Indian sandalwood oil.
