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(1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol is a complex terpenoid compound characterized by a naphthalene ring structure, multiple methyl and hydroxyl groups, and a pentenyl side chain. It is a derivative of decalin and exhibits biological activities, such as potential antimicrobial and antifungal properties.

26296-35-5

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26296-35-5 Usage

Uses

Used in Pharmaceutical Industry:
(1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol is used as a pharmaceutical compound for its potential antimicrobial and antifungal properties. Its complex structure and biological activities make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Industry:
(1R,8aα)-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1α-naphthalenemethanol is used as a chemical intermediate in the synthesis of various compounds due to its complex structure and functional groups. Its unique properties can be utilized in the development of new chemical products and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 26296-35-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,2,9 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 26296-35:
(7*2)+(6*6)+(5*2)+(4*9)+(3*6)+(2*3)+(1*5)=125
125 % 10 = 5
So 26296-35-5 is a valid CAS Registry Number.

26296-35-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 8(17)-kayadiol

1.2 Other means of identification

Product number -
Other names dehydropinifolic acid diol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:26296-35-5 SDS

26296-35-5Downstream Products

26296-35-5Relevant academic research and scientific papers

Agathadiol, a labdane diterpenoid from juniper berries, is a positive allosteric modulator of CB1R

Appendino, Giovanni,Khalili, Adil,Munoz, Eduardo,Pollastro, Federica,Salamone, Stefano,Unciti-Broceta, Juan D.

, (2021/10/27)

The neutral fraction of a juniper (Juniperus communis L.) berries acetone extract could positively modulate the activity of type 1 - cannabinoid receptor (CB1R). Bioactivity-directed fractionation identified the labdane diterpenoid agathadiol (4) as a positive allosteric modulator of CB1R, while closely related analogues were inactive. Agathadiol (4) is a minor constituent of juniper, but could be more conveniently obtained by semisynthesis from agathic acid (8), a major constituent of Manila copal.

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

Tanaka, Takashi,Kawamura, Keiko,Kitahara, Takumi,Kohda, Hiroshi,Tanaka, Osamu

, p. 615 - 622 (2007/10/02)

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

Raldugin, V. A.,Pentegova, V. A.

, p. 149 - 154 (2007/10/02)

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.

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