26296-35-5

Basic information

• Product Name: (1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol
• Synonyms: (1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol;Kayadiol
• CAS NO: 26296-35-5
• Molecular Formula: C20H34O2
• Molecular Weight: 306.48276
• Mol File: 26296-35-5.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol(26296-35-5)
• EPA Substance Registry System: (1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol(26296-35-5)

Safety Data

• Hazardous Substances Data: 26296-35-5(Hazardous Substances Data)

Usage

General Description

The chemical "(1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol" is a complex molecule that belongs to the class of terpenoid compounds. It contains a naphthalene ring structure and multiple methyl and hydroxyl groups, as well as a pentenyl side chain. This chemical is a derivative of decalin and is known to possess biological activities, including potential antimicrobial and antifungal properties. It is likely to have a significant impact on the chemical and pharmaceutical industries, given its complex structure and potential medicinal applications.

Upstream product

• 640-28-8 labda-8⁽¹⁷⁾,13-diene-15,19-dioic acid 
• 1757-85-3 dimethyl agathate 
• 14027-05-5 agathic acid 15-methyl ester 
• 640-28-8 agathic acid 
• 69308-72-1 isocupressic acid 
• 1909-96-2 methyl (E)-15-acetoxylabda-8⁽¹⁷⁾,13-dien-19-oate 
• 66471-92-9 Acetic acid (1S,4aS,5R,8aR)-5-((E)-5-acetoxy-3-methyl-pent-3-enyl)-1,4a-dimethyl-6-methylene-7-oxo-decahydro-naphthalen-1-ylmethyl ester 
• 3954-67-4 isocupressic acid methyl ester 
• 90374-84-8 dimethyl ester of 15-O-succinylisocupressic acid 
• 90527-77-8 methyl 18-acetoxyanticopulate 
• 86341-42-6 dimethyl 19-O-succinylagatholate 
• 66471-91-8 Villenatriol-15,19-diacetat 

Downstream Products

• 66471-77-0 villenol 

Relevant articles and documents

A NEW LABDANE ACID FROM THE NEEDLES OF Pinus sylvestris

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ENT-LABDANE-TYPE DITERPENE GLUCOSIDES FROM LEAVES OF RUBUS CHINGII

Previuosly, a sweet steviol bisglucoside named rubusoside was isolated from leaves of a Chinese Rubus spp. which was tentatively assigned as R. chingii.From leaves of Japanese Rubus chingii (Japanese name Gosho-Ichigo) which are not sweet, five ent-labdane-type diterpene glucosides named goshonosides F1-5 were isolated instead of rubososide and their structures were elucidated.The name 'R. suavissimus' has been proposed for the Chinese plant.Key Word Index - Rubus chingii; Rubus suavissimus; Rosaceae; glucosides of ent-labdane type diterpenes; goshonosides F1-5.

DERIVATIVES OF ANTICOPALIC ACID AND OTHER NEW COMPOUNDS FROM THE OLEORESIN OF Pinus pumila

From the oleoresin of the Japanese stone pine the previously known agatholic, agathalic, agathic and 3β-hydroxyanticopalic acids, and also the new acids 19-methoxyanticopalic and 19-O-succinylagatholic acids have been isolated and identified in the form of their methyl esters.Two new esters of 1-borneol have been isolated and characterized in the form of their acetates - the ferulate and the p-coumarate.