143249-79-0

Usage

Type of compound

Diol (contains two hydroxyl groups)

Azulene derivative

Yes (a bicyclic sesquiterpene with a deep blue color)

Isopropyl group

Present (attached to one of the carbon atoms)

Pharmaceutical and cosmetic industries

Commonly used for its anti-inflammatory and antioxidant properties

Skincare and dermatology products

Investigated for potential use

Inflammatory diseases

Studied for potential therapeutic effects in treatment

Versatile compound

Has various potential applications in medicine and personal care
This list provides a concise overview of the key characteristics and applications of 1,4-Azulenediol, 1,2,3,3a,4,5,6,8a-octahydro-1,4-dimethyl-7-(1-methylethyl)-.

Upstream product

• 34323-15-4 germacrene C 
• 257297-31-7 guaia-6,10(14)-dien-4-β-ol 
• 913707-11-6 (-)-10α-acetoxy-4β-hydroxy-1αH,5βH-guaia-6-ene 
• 862255-74-1 (-)-10α-acetoxy-1αH-guaia-4,6-dien-3-one 
• 913707-06-9 (-)-10α-acetoxy-1αH,5βH-guaia-3,6-diene 
• 913707-09-2 10α-acetoxy-3α-phenylselenyl-4β-hydroxy-1αH,5βH-guaia-6-ene 
• 913707-08-1 C₂₄H₃₂N₂O₄S 

Relevant academic research and scientific papers

Guaiane-type sesquiterpenoids from Alisma orientalis

Two guaiane-type sesquiterpenoids named orientalol E (1) and orientalol F (3) were isolated from the rhizome of Alisma orientalis (SAM) JUZEP together with two known guaiane-type sesquiterpenoids alismol (2) and alismoxide (4). Their relative stereo-struc

Syntheses of (+)-alismoxide and (+)-4-epi-alismoxide

(Chemical Equation Presented) The first total syntheses of (+)-alismoxide and (+)-4-epialismoxide are reported. Formal chemo-, regio-, and stereo-selective addition of water to 10α-acetoxy-1αH,5βH- guaia-3,6-diene afforded the target compounds after reduc

Marine Natural Products. IV. Chemical Constituents of an Okinawan Soft Coral of Xenia sp. (Xeniidae)

Four new polyhydroxysterols, named xeniasterol-a (4), xeniasterol-b (5), xeniasterol-c (6), and xeniasterol-d (7), were isolated from an Okinawan soft coral of Xenia sp. (Xeniidae).On the basis of chemical and physicochemical evidence, the structures of xeniasterol-a, -b, -c, and -d have been elucidated respectively as 7-O-acetylergost-22E-ene-3β,5α,6β,7β-tetraol (4), 7-O-acetylergosta-3β,5α,6β,7β-tetraol (5), gorgosta-3β,5α,6β-triol (6), and 7-O-acetylgorgosta-3β,5α,6β,7β-tetraol (7).Germacrene-c (1) was also isolated from the same soft coral together with two guaiane-type compounds (2,3), and it has been shown that germacrene-c (1) is readily air-oxidized to yield these cyclization products (2,3).Keywords-soft coral; Xenia sp.; Xeniidae; sterol polyhydroxylated; xeniasterol-a; xeniasterol-b; xeniasterol-c; xeniasterol-d; sesquiterpene; germacrene-c