5945-42-6

Usage

Uses

Used in Pharmaceutical Industry:
Aromaticin is used as a bioactive compound for its potential therapeutic effects. It has been found to exhibit anti-inflammatory, anti-cancer, and immunomodulatory properties, making it a promising candidate for the development of new drugs targeting various diseases.
Used in Cosmetic Industry:
Aromaticin is used as an active ingredient in the cosmetic industry for its potential skin-soothing and anti-inflammatory effects. It may be incorporated into skincare products to help reduce redness, irritation, and inflammation, providing a calming effect on the skin.
Used in Agricultural Industry:
Aromaticin may be used as a natural pesticide or fungicide in the agricultural industry due to its bioactive properties. It could potentially help protect crops from pests and diseases without the use of harsh chemicals, promoting a more sustainable and environmentally friendly approach to agriculture.
Used in Flavor and Fragrance Industry:
Due to its unique chemical structure, Aromaticin may also be used as a component in the flavor and fragrance industry. It could be utilized to create distinct and complex scents for perfumes, candles, and other aromatic products.

InChI:InChI=1/C15H18O3/c1-8-6-12-10(9(2)14(17)18-12)7-15(3)11(8)4-5-13(15)16/h4-5,8,10-12H,2,6-7H2,1,3H3/t8-,10-,11+,12+,15+/m1/s1

Upstream product

• 60403-31-8 (3aS,4aR,5R,7aR,8S,9aR)-5-tert-Butoxy-4a,8-dimethyl-3-methylene-decahydro-azuleno[6,5-b]furan-2-one 
• 146644-15-7 (+/-)-4-methyl-1,2,3,4,5,8-hexahydro-1-oxoazulene-7-ethanol 
• 146644-12-4 (+/-)-4-methyl-7-methylene-3,4,5,6,7,8-hexahydroazulen-1(2H)-one 
• 6605-59-0 2,3-dihydroaromaticin 
• 123130-59-6 3-(1-methylethenyl)-2-<2-<(trimethylsilyl)methyl>allyl>-2-cyclopenten-1-one 
• 60403-28-3 dec-t-5-yl> acetic acid-γ-lactone 
• 68197-11-5 c-2,t-7-dimethyl-t-8-(t-butyloxy)-r-1H-bicyclo<5.3.0>decan-5-one 
• 74615-15-9 ((3S,3aS,8R,8aS)-3-tert-Butoxy-3a,8-dimethyl-1,2,3,3a,4,7,8,8a-octahydro-azulen-5-yl)-acetic acid methyl ester 
• 74615-16-0 (1R,3aR,4S,6R,7S,8aR)-1-tert-Butoxy-7-(2-hydroxy-ethyl)-4,8a-dimethyl-decahydro-azulen-6-ol 

Downstream Products

• 96598-30-0 Benzoic acid (3R,3aR,4aS,5R,7S,7aS,8R,9aS)-7-acetoxy-3,4a,8-trimethyl-2-oxo-dodecahydro-azuleno[6,5-b]furan-5-yl ester 
• 6754-35-4 pulchellin 

Relevant academic research and scientific papers

Allylsilane-Based Annulations. Direct Stereoselective Syntheses of (+/-)-Graveolide and (+/-)-Aromaticin

An allylsilane-based annulation was used to construct a functionalized perhydroazulene.The C(1), C(5), and C(10) stereocenters, characteristic of the helenanolides, were established using a reductive alkylation strategy.Stereoselective syntheses of the pseudoguaianolides graveolide and aromaticin were achieved.