79902-60-6 Usage
Description
[(1S,3S,7S,8R,8aS)-8-[2-[(2R,4R)-4-hydroxy-6-oxo-oxan-2-yl]ethyl]-3,7dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-ethyl-2-methyl-butan oate is a complex organic ester compound with a long and intricate chemical structure. It is derived from naphthalene and contains various functional groups, including hydroxyl and oxan-2-yl, as well as methyl and ethyl groups. [(1S,3S,7S,8R,8aS)-8-[2-[(2R,4R)-4-hydroxy-6-oxo-oxan-2-yl]ethyl]-3,7dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-ethyl-2-methyl-butan oate's unique structure and functional groups make it a potential candidate for applications in the pharmaceutical or chemical industries.
Uses
Used in Pharmaceutical Industry:
[(1S,3S,7S,8R,8aS)-8-[2-[(2R,4R)-4-hydroxy-6-oxo-oxan-2-yl]ethyl]-3,7dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-ethyl-2-methyl-butan oate is used as a potential pharmaceutical compound for [application reason]. Its complex structure and functional groups may offer unique properties that can be harnessed for the development of new drugs or therapies.
Used in Chemical Industry:
In the chemical industry, [(1S,3S,7S,8R,8aS)-8-[2-[(2R,4R)-4-hydroxy-6-oxo-oxan-2-yl]ethyl]-3,7dimethyl-1,2,3,7,8,8a-hexahydronaphthalen-1-yl] 2-ethyl-2-methyl-butan oate is used as a [application type] for [application reason]. Its specific functional groups and structural features may be utilized in the synthesis of other complex molecules or as intermediates in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 79902-60-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,9,0 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 79902-60:
(7*7)+(6*9)+(5*9)+(4*0)+(3*2)+(2*6)+(1*0)=166
166 % 10 = 6
So 79902-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C26H40O5/c1-6-26(5,7-2)25(29)31-22-13-16(3)12-18-9-8-17(4)21(24(18)22)11-10-20-14-19(27)15-23(28)30-20/h8-9,12,16-17,19-22,24,27H,6-7,10-11,13-15H2,1-5H3/t16-,17-,19-,20-,21-,22+,24-/m1/s1
79902-60-6Relevant articles and documents
3-Hydroxy-3-methylglutaryl-coenzyme A Reductase Inhibitors. 4. Side Chain Ester Derivatives of Mevinolin
Hoffman, W. F.,Alberts, A. W.,Anderson, P. S.,Chen, J. S.,Smith, R. L.,Willard, A. K.
, p. 849 - 852 (2007/10/02)
Modification of the 2(S)-methylbutyryl moiety of mevinolin led to a series of side chain ester derivatives.A systematic exploration of the structure-activity relationships showed that the introduction of an additional aliphatic group on the carbon α to the carbonyl group increased potency.This obsrevation led to the synthesis of compound 16, which has about 2.5 times the intrinsic inhibitory activity of mevinolin.
