87879-56-9 Usage
Uses
Used in Organic Chemistry:
(6R,14R,22R,30R,32S)-6,14,22,30,32-pentahydroxytritriacontane-8,16,24-trione is used as a building block for the synthesis of more complex organic molecules due to its unique structure and functional groups.
Used in Biochemistry:
(6R,14R,22R,30R,32S)-6,14,22,30,32-pentahydroxytritriacontane-8,16,24-trione is used as a potential candidate for the development of new bioactive compounds, given its complex structure and functional groups that can interact with biological systems.
Used in Pharmaceutical Industry:
(6R,14R,22R,30R,32S)-6,14,22,30,32-pentahydroxytritriacontane-8,16,24-trione is used as a starting material for the development of new drugs, as its unique structure and functional groups may provide novel pharmacological properties.
Used in Material Science:
(6R,14R,22R,30R,32S)-6,14,22,30,32-pentahydroxytritriacontane-8,16,24-trione is used as a component in the development of new materials, such as polymers or coatings, due to its unique structural properties and functional groups.
Used in Chemical Research:
(6R,14R,22R,30R,32S)-6,14,22,30,32-pentahydroxytritriacontane-8,16,24-trione is used as a subject of study in chemical research to better understand its properties, reactivity, and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 87879-56-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,8,7 and 9 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87879-56:
(7*8)+(6*7)+(5*8)+(4*7)+(3*9)+(2*5)+(1*6)=209
209 % 10 = 9
So 87879-56-9 is a valid CAS Registry Number.
87879-56-9Relevant academic research and scientific papers
Highly stereoselective total synthesis of PM-Toxin B, a corn host-specific pathotoxin
Hosaka, Mitsuru,Hayakawa, Hiroyuki,Miyashita, Masaaki
, p. 4227 - 4230 (2007/10/03)
The highly stereoselective total synthesis of PM-toxin B, a corn host-specific toxin produced by the fungal pathogen Phyllosticta maydis, has been achieved by a convergent synthetic strategy which involves cross-aldol coupling of four key segments and the