53584-59-1 Usage
Classification
Trinorhopane It is a type of triterpene, which is a large group of natural organic compounds derived from plants and animals.
Structure
Bicyclic triterpene It has a unique structure consisting of two interconnected rings, which contributes to its properties and potential applications.
Family
Norhopane It belongs to the norhopane family, which is derived from the hopane skeleton, a common structure found in many natural triterpenes.
Applications
Medicinal chemistry, pharmacology, and organic synthesis Due to its unique structure and properties, 17alpha(H)-22,29,30-Trisnorhopane has potential applications in various fields, including the development of new drugs and the synthesis of complex organic compounds.
Biological activities
It is known for its biological activities, which may include interactions with cellular receptors, enzymes, or other biological targets.
Reference compound
Analytical chemistry and pharmaceutical research 17alpha(H)-22,29,30-Trisnorhopane is used as a reference compound in these fields, helping researchers to compare and analyze the properties of other related compounds.
Synthesis and isolation
Scientific community interest The synthesis and isolation of 17alpha(H)-22,29,30-Trisnorhopane have attracted attention from researchers, who are interested in understanding its properties and potential applications.
Ongoing research
Potential applications The scientific community continues to explore the potential applications of 17alpha(H)-22,29,30-Trisnorhopane, as its unique structure and properties may lead to new discoveries and advancements in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 53584-59-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,8 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53584-59:
(7*5)+(6*3)+(5*5)+(4*8)+(3*4)+(2*5)+(1*9)=141
141 % 10 = 1
So 53584-59-1 is a valid CAS Registry Number.
InChI:InChI=1/C27H46/c1-23(2)14-8-16-25(4)20(23)13-18-27(6)22(25)11-10-21-24(3)15-7-9-19(24)12-17-26(21,27)5/h19-22H,7-18H2,1-6H3
53584-59-1Relevant articles and documents
Synthesis of Biological Markers in Fossil Fuels. 3. Degraded and Rearranged C27 Hopanes
Dunlap, Norma K.,Sabol, Mark R.,Bauer, Philip E.,Watt, David S.,Reibenspies, Joseph H.,et al.
, p. 1826 - 1829 (2007/10/02)
22-Hydroxyhopan-3-one was converted to various C27 hopane hydrocarbons: 22,29,30-trinorhopane, 22,29,30-trinor-17α-hopane, 22,29,30-trinor-28(18 -> 17S)abeo-13α,18β-hopane, and 22,29,30-trinor-28(18 -> 17S)abeo-13α,18α-hopane.These hydrocarbons are useful as biological markers in studies related to the source, maturation, and migration of crude oils.