4545-68-0

Usage

Uses

Used in Traditional Chinese Medicine:
(-)-ALPHA-NEOCLOVENE is used as a medicinal component in traditional Chinese medicine for its potential therapeutic properties. It is believed to contribute to the overall efficacy of ginseng-based remedies, which have been used for centuries to treat various ailments and promote overall health and well-being.
Used in Aromatherapy:
(-)-ALPHA-NEOCLOVENE is used as a fragrance ingredient in aromatherapy for its strong aroma. Its volatile nature allows it to be easily diffused in the air, creating a pleasant and invigorating scent that can have a positive impact on mood and well-being.
Used in Flavor and Fragrance Industry:
In the flavor and fragrance industry, (-)-ALPHA-NEOCLOVENE is used as a key component in the creation of various scent profiles and flavor formulations. Its unique aroma can be incorporated into perfumes, candles, and other scented products to enhance their overall appeal and create a distinct olfactory experience.
Used in Cosmetics and Personal Care Products:
(-)-ALPHA-NEOCLOVENE is used as a natural ingredient in cosmetics and personal care products, such as skincare and hair care formulations. Its strong aroma can provide a pleasant scent to these products, while its potential therapeutic properties may contribute to their overall effectiveness in promoting skin and hair health.

InChI:InChI=1/C15H24/c1-11-6-5-8-14(4)12-7-9-15(11,14)10-13(12,2)3/h6,12H,5,7-10H2,1-4H3/t12-,14-,15?/m0/s1

Upstream product

• 87-44-5 β-caryophyllene 
• 80374-27-2 (2aS,4aR,8R,8aS)-2,2,4a,,8-tetramethyldecahydrocyclobutinden-8-ol 

Downstream Products

• 117591-80-7 ginsenol 
• 137235-60-0 4-Bromo-benzoic acid (1R,2S,2aR,4aR,7aS,7bR)-2-hydroxy-2,2a,4a,7a-tetramethyl-decahydro-cyclopenta[cd]inden-1-yl ester 

Relevant academic research and scientific papers

Acid-catalyzed isomerization of caryophyllene in the presence of SiO2 and Al2O3 impregnated with sulfuric acid

The conversion of caryophyllene upon contact with Al2O3 and SiO2 impregnated with sulfuric acid was carried out, and the components of the resulting mixtures were identified. Having in hands such “standard” mixtures greatl

Rearrangement of (-)-β-caryophyllene. A product analysis and force field study

The rearrangement of (-)-β-caryophyllene (1) with sulfuric acid in ether has been reinvestigated. In the early stage, a multitude of products is formed. Of these, fourteen hydrocarbons (3, 4, 6-17) and four alcohols (5, 18-20) were obtained pure. From the very beginning, the tricycloundecenes 15-17 assumulate quickly. This indicates that a previously unknown rearrangement of 1 by protonation of the exocyclic double bond followed by transannular ring closure is a main reaction, and that the conformation βα is involved. Three hydrocarbons (3, 4, 8) and three alcohols (5, 18, 19) proved to be stable. They are the main components in the late stage. A complete rearrangement scheme followed from a force field analysis using MMP2. First, all conformations up to 4 kcal above the global minimum of each product and each carbenium ion necessary for its formation were detected automatically using the search program HUNTER. Second, the conformation favoring a specific transformation was searched for. For transannular cyclizations, the conformation with the shortest distance between the atoms to be bound and, for ring openings and 1,2-shifts, the conformation with the smallest dihedral angle between the empty p-orbital and the bond to be broken were selected. In all cases, the selection criteria proved valid: The stereochemistry of the conformations selected matched the stereochemistry of the products observed. On the basis of the results presented, a fully automated search program for favorable rearrangement paths may be developed.