59812-47-4 Usage
Uses
Used in Pharmaceutical Industry:
(3R)-3,4,5,5a,6,7,8,9-Octahydro-2,2,5aβ,9β-tetramethyl-2H-3β,9aβ-methano-1-benzoxepine-5α,6β,7β-triol is used as a potential pharmaceutical agent due to its complex structure and the presence of various functional groups. Its specific molecular configuration may allow it to interact with biological targets, making it a candidate for the development of new drugs or therapeutic agents.
Used in Chemical Research:
In the field of chemical research, (3R)-3,4,5,5a,6,7,8,9-Octahydro-2,2,5aβ,9β-tetramethyl-2H-3β,9aβ-methano-1-benzoxepine-5α,6β,7β-triol serves as a subject of study for understanding the synthesis, reactivity, and properties of complex organic molecules. Its unique structure may provide insights into new chemical reactions or mechanisms, contributing to the advancement of organic chemistry.
Used in Material Science:
(3R)-3,4,5,5a,6,7,8,9-Octahydro-2,2,5aβ,9β-tetramethyl-2H-3β,9aβ-methano-1-benzoxepine-5α,6β,7β-triol may also find applications in material science, where its complex structure and functional groups could be leveraged to develop new materials with specific properties. These materials could have uses in various industries, such as electronics, coatings, or advanced materials for specialized applications.
Check Digit Verification of cas no
The CAS Registry Mumber 59812-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,8,1 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 59812-47:
(7*5)+(6*9)+(5*8)+(4*1)+(3*2)+(2*4)+(1*7)=154
154 % 10 = 4
So 59812-47-4 is a valid CAS Registry Number.
59812-47-4Relevant academic research and scientific papers
STEREOSELECTIVE TOTAL SYNTHESIS OF (+/-)-ISOCELORBICOL
Huffman, John W.,Raveendranath, Panolil C.
, p. 5557 - 5566 (2007/10/02)
A completely stereoselective total synthesis of the naturally occuring polyhydroxyagarofuran, (+/-)-isocelorbicol (1) is described.The readily available α-agarofuran derivative 3 was converted to 3β-hydroxy-9-keto-β-agarofuran (6) by epoxidation followed
