115-71-9 Usage
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 5-(2,3-dimethyltricyclo[2.2.1.02,6]hept-3-yl)-2-methylpent-2-en-1-ol, stereoisomer 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
Identification of &α-Santalenoic and endo-&β-Bergamotenoic Acids as Moth Oviposition Stimulants from Wild Tomato Leaves
Coates, Robert M.,Denissen, Jon F.,Juvik, John A.,Babka, Barbara A.
, p. 2186 - 2192 (2007/10/02)
The presence of oviposition-stimulating phytochemicals in hexane extracts of whole leaves of wild tomato (Lycopersicon hirsutum) accession LA 1777 was indicated by oviposition preference assays with gravid female Heliothis zea (Boddie) moths.Three sesquiterpenes isolated from these extracts were identified as (+)-(E)-α-santalen-12-oic acid (1a), (+)-(E)-endo-β-bergamoten-12-oic acid (2a), and (-)-(E)-endo-α-bergamoten-12-oic acid (3a).Structure assignments based primarily on 1H and 13C NMR spectral interpretations were confirmed by conversion to the parent sesquiterpene hydrocarbons and subsequent comparisons with authentic endo-β-bergamotene and/or literature data.The identity of 1a was verified by comparison of its methyl ester (1b) with a sample synthesized from (+)-α-santalol (9).Quantitative assays demonstrated that the two major sesquiterpene acids, 1a and 2a, are the principal oviposition stimulants in the tomato leaf extracts and that the activity of 2a is about twice that of 1a.
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.
A Direct Synthesis of Z-Trisubstituted Allylic Alcohols via the Wittig Reaction
Sreekumar, C.,Darst, Kevin P.,Still, W. Clark
, p. 4260 - 4262 (2007/10/02)
The lithium-free modification of the Wittig reaction of unstabilized ylides and acyclic α-alkoxy ketones leads to protected trisubstituted allylic alcohols with high stereoselectivity for the Z isomer.
