61494-73-3 Usage
General Description
The chemical 12-hydroxyabieta-8(14),9(11),12-triene-3,7-dione is a diterpenoid compound found in various plants and is known for its anti-inflammatory and antioxidant properties. It has been studied for its potential therapeutic effects on various diseases, including cancer, due to its ability to inhibit the growth of cancer cells and induce cell death. Additionally, it has demonstrated antibacterial and antifungal activities, making it a potential candidate for the development of new antimicrobial agents. Furthermore, 12-hydroxyabieta-8(14),9(11),12-triene-3,7-dione has been found to have neuroprotective effects, making it a promising compound for the treatment of neurodegenerative diseases. Further research is needed to fully understand the potential uses and mechanisms of action of 12-hydroxyabieta-8(14),9(11),12-triene-3,7-dione.
Check Digit Verification of cas no
The CAS Registry Mumber 61494-73-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,4,9 and 4 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61494-73:
(7*6)+(6*1)+(5*4)+(4*9)+(3*4)+(2*7)+(1*3)=133
133 % 10 = 3
So 61494-73-3 is a valid CAS Registry Number.
61494-73-3Relevant academic research and scientific papers
Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta-8,11,13-triene
Burnell, Robert H.,Caron, Stephane
, p. 1446 - 1454 (2007/10/02)
An approach to the synthesis of aromatic diterpenes was tested for its generality.Phenylacetonitriles with increasing substitution on the aromatic ring were prepared and alkylated with geranyl bromide and the resulting dienes subjected to cationic cycliza
Synthesis of aromatic diterpenes synthesis of 12-hydroxy-abieta-8,11,13-trien-3,7-dione
Burnell,Caron
, p. 127 - 132 (2007/10/02)
Model studies involving cationic cyclisation of suitable dienes have provided a synthesis of the title compound. Preparation of the dienes from available aromatic starting materials and the modification of the cyclised products are described.
