668-49-5 Usage
Description
4-(3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid is a complex organic compound characterized by its pentanoic acid structure and a unique tetradecahydro-cyclopenta[a]phenanthren-17-yl group. This molecule features multiple hydroxyl and methyl groups, which may contribute to its potential applications in various fields.
Uses
Used in Pharmaceutical Industry:
4-(3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid is used as a potential pharmaceutical compound for its unique structural features. The presence of hydroxyl and methyl groups may allow for interactions with specific biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, this compound can be used as a starting material or a building block for the synthesis of more complex molecules. Its unique structure may provide insights into the development of new chemical reactions or the creation of novel molecular architectures.
Used in Analytical Chemistry:
As a complex organic molecule, 4-(3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid can be employed as a standard or reference compound in analytical chemistry. It may be used to calibrate instruments or to validate analytical methods, particularly those involving the analysis of complex organic mixtures.
Used in Material Science:
The unique structural features of this compound may also find applications in material science, where it could be used to develop new materials with specific properties. For example, its hydroxyl and methyl groups could be exploited to create self-assembling structures or to modify the surface properties of materials.
Used in Environmental Science:
In environmental science, this compound could be studied for its potential role in the biodegradation of complex organic pollutants or for its ability to interact with environmental contaminants. Understanding its behavior in the environment could lead to the development of new strategies for pollution control and remediation.
Please note that the specific applications mentioned above are hypothetical and based on the structural features of the compound. The actual uses of 4-(3,6-dihydroxy-10,13-dimethyl-2,3,4,5,6,7,8,9,11,12,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-17-yl)pentanoic acid would depend on further research and development in the relevant fields.
Check Digit Verification of cas no
The CAS Registry Mumber 668-49-5 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,6 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 668-49:
(5*6)+(4*6)+(3*8)+(2*4)+(1*9)=95
95 % 10 = 5
So 668-49-5 is a valid CAS Registry Number.
InChI:InChI=1/C24H40O4/c1-14(4-7-22(27)28)17-5-6-18-16-13-21(26)20-12-15(25)8-10-24(20,3)19(16)9-11-23(17,18)2/h14-21,25-26H,4-13H2,1-3H3,(H,27,28)/t14-,15-,16+,17-,18+,19+,20+,21-,23-,24-/m1/s1
668-49-5Relevant articles and documents
Catalytic oxidations of steroid substrates by artificial cytochrome p-450 enzymes.
Yang, Jerry,Gabriele, Bartolo,Belvedere, Sandro,Huang, Ying,Breslow, Ronald
, p. 5057 - 5067 (2007/10/03)
Catalysts comprising manganese-porphyrins carrying cyclodextrin binding groups are able to perform hydroxylations with substrate selectivity and regio- and stereoselectivity and high catalytic turnovers. The geometries of the catalyst/substrate complexes override intrinsic substrate reactivities, permitting attack on geometrically accessible saturated carbons of steroids in the presence of secondary carbinol groups and carbon-carbon double bonds, as in enzymatic reactions. Selective hydroxylations of steroid carbon 9 positions are of particular practical interest.
