1857-24-5 Usage
Uses
Used in Organic Synthesis:
[1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol is used as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure and functional groups make it a valuable building block for the development of novel compounds.
Used in Biochemistry:
In the field of biochemistry, [1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol may be utilized as a probe or a reagent to study the interactions and mechanisms of biological systems. Its specific stereochemistry could provide insights into enzyme specificity and substrate recognition.
Used in Pharmacology:
[1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol has potential applications in pharmacology, where its unique structure and functional groups could be exploited to develop new drugs or drug candidates. [1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol's properties may be harnessed to target specific biological pathways or receptors, leading to the development of innovative therapeutics.
Used in the Fragrance Industry:
Given its complex and potentially fragrant structure, [1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol could be used as a component in the creation of unique fragrances and perfumes, adding depth and complexity to the final product.
Used in the Chemical Industry:
[1S,8aα,(+)]-Decahydro-5β-[(E)-5-hydroxy-3-methyl-3-pentenyl]-1,4aβ-dimethyl-6-methylene-1-naphthalenemethanol's unique structure and functional groups may also find applications in the chemical industry for the development of specialty chemicals, materials, or coatings that require specific properties derived from its molecular architecture.
Check Digit Verification of cas no
The CAS Registry Mumber 1857-24-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,8,5 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1857-24:
(6*1)+(5*8)+(4*5)+(3*7)+(2*2)+(1*4)=95
95 % 10 = 5
So 1857-24-5 is a valid CAS Registry Number.
1857-24-5Relevant 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.
