14772-54-4 Usage
Description
(3S,9R,10S,13R,14S,17R)-3-hydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-14-carbaldehyde is a complex organic compound with a unique molecular structure. It is a steroid derivative characterized by a cyclic structure with multiple carbon rings and various functional groups, including hydroxyl, methyl, and carbonyl groups. The presence of the carbaldehyde group suggests potential reactivity and the ability to participate in chemical reactions.
Uses
Used in Pharmaceutical Industry:
(3S,9R,10S,13R,14S,17R)-3-hydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-14-carbaldehyde is used as a potential pharmaceutical candidate due to its complex molecular structure and the presence of various functional groups. Its steroidal nature and reactivity may offer opportunities for the development of new drugs and therapeutic agents.
Used in Chemical Industry:
In the chemical industry, (3S,9R,10S,13R,14S,17R)-3-hydroxy-4,4,10,13-tetramethyl-17-[(2R)-6-methylheptan-2-yl]-2,3,5,6,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-14-carbaldehyde may be utilized as a building block or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups could be valuable in creating new chemical products or improving existing ones.
Further research is needed to fully understand the properties and potential uses of this compound in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 14772-54-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,7 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 14772-54:
(7*1)+(6*4)+(5*7)+(4*7)+(3*2)+(2*5)+(1*4)=114
114 % 10 = 4
So 14772-54-4 is a valid CAS Registry Number.
InChI:InChI=1/C30H50O2/c1-20(2)9-8-10-21(3)22-14-18-30(19-31)24-11-12-25-27(4,5)26(32)15-16-28(25,6)23(24)13-17-29(22,30)7/h11,19-23,25-26,32H,8-10,12-18H2,1-7H3/t21-,22-,23+,25?,26+,28-,29-,30-/m1/s1
14772-54-4Relevant articles and documents
Synthesis of 14-&α-Aminomethyl substituted Lanosterol Derivatives; Inhibitors of Fungal Ergosterol Biosynthesis
Cooper, Alan B.,Wright, John J.,Ganguly, Ashit K.,Desai, Jagdish,Loebenberg, David,et al.
, p. 898 - 900 (1989)
Several 14-α-aminomethyl-substituted lanosterol derivatives have been synthesized involving a complete Δ7,8 to Δ8,9 isomerization; these compounds are inhibitors of fungal ergosterol biosynthesis and are active against intact Candida and dermatophyte strains.
STEROIDAL 14ALPHA-CARBOXY-ALKYL DERIVATIVES AS REGULATORS OF HMG-COA REDUCTASE
-
, (2008/06/13)
New 14α-carboxyalkyl sterols are regulators of HMG-CoA reductase and inhibitors of mammalian 14α-methyl demethylase and are useful in lowering serum cholesterol levels and treating fungal infections.
The synthesis of some 32-functionalised lanostane derivatives.
Batten,Bentley,Boar,Draper,McGhie,Barton
, p. 739 - 748 (2007/10/04)
-
