102848-61-3 Usage
Uses
Used in Pharmaceutical Research:
(5S,9S,10S,13R)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one is used as a potential candidate in pharmaceutical research for the development of new drugs. Its unique molecular structure and steroidal nature may offer novel therapeutic applications.
Used in Analytical Chemistry:
(5S,9S,10S,13R)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahydrocyclopenta[a]phenanthren-3-one is used as a reference standard in analytical chemistry. Its distinct chemical properties and structure make it a valuable tool for calibration and quality control in various analytical techniques.
Further studies may be required to fully understand the chemical and biological properties of (5S,9S,10S,13R)-4,4,8,10,14-pentamethyl-1,2,5,6,7,9,11,12,13,15-decahy drocyclopenta[a]phenanthren-3-one, which could lead to additional applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 102848-61-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,8,4 and 8 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 102848-61:
(8*1)+(7*0)+(6*2)+(5*8)+(4*4)+(3*8)+(2*6)+(1*1)=113
113 % 10 = 3
So 102848-61-3 is a valid CAS Registry Number.
InChI:InChI=1/C22H34O/c1-19(2)16-10-14-22(5)17(20(16,3)13-11-18(19)23)9-8-15-7-6-12-21(15,22)4/h6-7,15-17H,8-14H2,1-5H3/t15-,16-,17+,20-,21?,22?/m0/s1
102848-61-3Relevant academic research and scientific papers
Provan, Gordon J.,Waterman, Peter G.
, p. 917 - 922 (1986)
Key Word Index - Commiphora insica; Burseraceae; resin; dammaranes; 16(S),20(R)-dihydroxydammar-24-en-3-one; 17-octanordammaranes; mansumbinone; mansumbinol; 3,4-seco-mansumbinoic acid.The resin of Commiphora incisa (Burseraceae) has yielded three C22 compounds derived by loss of the C-17 side chain from a dammarane triterpene.They have been identified by spectral analysis and chemical modification as 4α,4β,8β,10β,14α-pentamethyl-5α-gon-16-en-3-one (mansumbinone), the corresponding 3-hydroxy compound (mansumbinol) and the derivative 3,4-seco-mansumbinoic acid in which the A-ring has opened between C-3 and C-4.A fourth compound was characterized as 16(S),20(R)-dihydroxydammar-24-en-3-one, a possible precursor of the mansumbinanes.
