1227-93-6 Usage
Uses
Used in Pharmaceutical Industry:
(3S,6aα,10bα)-Dodecahydro-3,4aβ,7,7,10aβ-pentamethyl-3β-vinyl-1H-naphtho[2,1-b]pyran is used as a potential pharmaceutical compound for its unique chemical structure. (3S,6aα,10bα)-Dodecahydro-3,4aβ,7,7,10aβ-pentamethyl-3β-vinyl-1H-naphtho[2,1-b]pyran's complex arrangement of atoms and rigid three-dimensional shape may offer novel interactions with biological targets, making it a candidate for the development of new drugs or therapies.
Used in Chemical Research:
In the field of chemical research, (3S,6aα,10bα)-Dodecahydro-3,4aβ,7,7,10aβ-pentamethyl-3β-vinyl-1H-naphtho[2,1-b]pyran serves as a subject of study for understanding its chemical properties and reactivity. The molecule's unique structure may provide insights into new reaction mechanisms or catalysis processes, contributing to the advancement of organic chemistry.
Used in Material Science:
(3S,6aα,10bα)-Dodecahydro-3,4aβ,7,7,10aβ-pentamethyl-3β-vinyl-1H-naphtho[2,1-b]pyran may also find applications in material science, where its rigid structure and unique arrangement of atoms could be exploited to create new materials with specific properties, such as improved strength, stability, or chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 1227-93-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,2 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1227-93:
(6*1)+(5*2)+(4*2)+(3*7)+(2*9)+(1*3)=66
66 % 10 = 6
So 1227-93-6 is a valid CAS Registry Number.
1227-93-6Relevant academic research and scientific papers
Microbial Transformation of Manool and (12Z)-Labda-8(17),12,14-triene by Rhodococcus erythropolis JTS-131
Hieda, Tadaharu,Mikami, Yoichi,Obi, Yukiteru
, p. 787 - 794 (2007/10/02)
Rhodococcus erythropolis JTS-131, a cis-abienol and sclareol transformable bacterium, converted manool and accumulated manoyl oxide in the culture broth.In the presence of metabolic inhibitors, 13β-hydroxylabda-8(17),14-dien-18-oic acid and its methylester (a new compound) were accumulated as the transformation products.This strain also transformed (12Z)-labda-8(17),12,14-triene and accumulated (12Z)-labda-8(17),12,14-trien-18-al in the culture broth.In the presence of metabolic inhibitors, two compounds, (12Z)-labda-8(17),12,14-trien-18-ol and 4,18,19-trinor-3,4-seco-5-oxo-(12Z)-labda-8(17),12,14-trien-3-oic acid were accumulated.Based on the experiments on the degradation sequence, transformation pathways for these two labdanes by the bacterium are proposed.
