33947-55-6 Usage
Uses
Used in Pharmaceutical Industry:
(1S,4aα,αR)-Decahydro-α-vinyl-5α-(hydroxymethyl)-α,5,8aβ-trimethyl-2-methylene-1-naphthalene-1-propanol is used as a precursor compound for the synthesis of various pharmaceutical agents. Its complex structure and reactivity make it a valuable component in the development of new drugs and medicinal compounds.
Used in Chemical Industry:
In the chemical industry, (1S,4aα,αR)-Decahydro-α-vinyl-5α-(hydroxymethyl)-α,5,8aβ-trimethyl-2-methylene-1-naphthalene-1-propanol is utilized as a building block for the creation of other organic compounds. Its specific properties allow it to be a key intermediate in chemical reactions, contributing to the formation of a wide range of products.
Given the complexity of the compound and the lack of specific details on its applications, these uses are based on the general knowledge of similar organic compounds and their typical roles in the pharmaceutical and chemical industries. Further research and development would be necessary to fully understand the specific applications and potential of (1S,4aα,αR)-Decahydro-α-vinyl-5α-(hydroxymethyl)-α,5,8aβ-trimethyl-2-methylene-1-naphthalene-1-propanol.
Check Digit Verification of cas no
The CAS Registry Mumber 33947-55-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,9,4 and 7 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33947-55:
(7*3)+(6*3)+(5*9)+(4*4)+(3*7)+(2*5)+(1*5)=136
136 % 10 = 6
So 33947-55-6 is a valid CAS Registry Number.
33947-55-6Relevant 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.
