19903-73-2 Usage
Description
(-)-EPICEDROL, also known as (2R,7R)-2,6,6,8-tetramethyltricyclo[5.3.1.0^1,5]undecan-8-ol, is a new natural product extracted from Asphodelus albus roots. It is defined as the 8S-epimer of cedrol, a compound with potential applications in various industries.
Uses
Used in Pharmaceutical Industry:
(-)-EPICEDROL is used as a pharmaceutical compound for its potential therapeutic properties. The compound's unique structure and natural origin make it a promising candidate for the development of new drugs and treatments.
Used in Chemical Research:
(-)-EPICEDROL is used as a research compound for studying its chemical properties and potential interactions with other molecules. This can lead to a better understanding of its applications and the development of new compounds with similar or improved properties.
Used in Natural Product Extraction:
(-)-EPICEDROL is used as a natural product extracted from Asphodelus albus roots, which can be further studied and utilized in various applications, such as in the development of new drugs, cosmetics, or other products that benefit from its unique properties.
Check Digit Verification of cas no
The CAS Registry Mumber 19903-73-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,0 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19903-73:
(7*1)+(6*9)+(5*9)+(4*0)+(3*3)+(2*7)+(1*3)=132
132 % 10 = 2
So 19903-73-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-10-5-6-11-13(2,3)12-9-15(10,11)8-7-14(12,4)16/h10-12,16H,5-9H2,1-4H3/t10-,11+,12-,14+,15+/m1/s1
19903-73-2Relevant articles and documents
Ruthenium-Catalyzed C-H Bond Activation. Oxyfunctionalization of Nonactivated C-H Bonds in the Cedrane Series with RuO4 Generated in Situ
Tenaglia, A.,Terranova, E.,Waegell, B.
, p. 5523 - 5528 (1992)
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RUTHENIUM-CATALYZED C-H BOND ACTIVATION OXIDATION OF BRIDGED BICYCLIC AND TRICYCLIC ALKANES
Tenaglia, A.,Terranova, E.,Waegell, B.
, p. 5271 - 5274 (2007/10/02)
Catalytic oxydation (hydroxylation) with RuO4 generated in situ occurs preferentially in tertiary position with retention of configuration on various bicyclic or tricyclic alcanes.
