87833-53-2 Usage
Uses
Used in Pharmaceutical Industry:
(4aR,6aS,13aR,13bS)-12-methoxy-4,4,6a,8,13b-pentamethyl-1,4,4a,5,6,6a,9,13,13a,13b-decahydro-2H-benzo[a]furo[3,4-i]xanthene-3,11-dione is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure may offer novel mechanisms of action for treating various diseases and conditions, pending further research and clinical trials.
Used in Agrochemical Industry:
In the agrochemical industry, (4aR,6aS,13aR,13bS)-12-methoxy-4,4,6a,8,13b-pentamethyl-1,4,4a,5,6,6a,9,13,13a,13b-decahydro-2H-benzo[a]furo[3,4-i]xanthene-3,11-dione may be utilized as an active ingredient in pesticides or herbicides. Its complex structure could provide new ways to control pests and weeds, contributing to more effective and targeted agricultural solutions.
Used in Materials Science:
(4aR,6aS,13aR,13bS)-12-methoxy-4,4,6a,8,13b-pentamethyl-1,4,4a,5,6,6a,9,13,13a,13b-decahydro-2H-benzo[a]furo[3,4-i]xanthene-3,11-dione is used in materials science for its potential to contribute to the development of new materials with unique properties. Its chemical structure may enable the creation of advanced materials for various applications, such as in electronics, optics, or nanotechnology, subject to ongoing research and development.
Check Digit Verification of cas no
The CAS Registry Mumber 87833-53-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,3 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87833-53:
(7*8)+(6*7)+(5*8)+(4*3)+(3*3)+(2*5)+(1*3)=172
172 % 10 = 2
So 87833-53-2 is a valid CAS Registry Number.
87833-53-2Relevant academic research and scientific papers
Ma, Tsz-Kan,Parsons, Philip J.,Barrett, Anthony G. M.
, p. 4961 - 4970 (2019)
The first total synthesis of five austalide natural products, (±)-17S-dihydroaustalide K, (±)-austalide K, (±)-13-deacetoxyaustalide I, (±)-austalide P, and (±)-13-deoxyaustalide Q acid, was accomplished via a series of biomimetic transformations. Key ste