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CAS 125142-16-7

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2,2-Dimethyl-butanoic Acid [1S-[1a,3a,4aa,7,8(2S*,4S*),8a]]-8-[2-[4-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]tetrahydro-6-oxo-2H-pyran-2-yl]ethyl]-1,2,3,4,4a,7,8,8a-octahydro-4a-hydroxy-3,7-dimethyl-1-naphthalenyl Ester

Description:
2,2-Dimethyl-butanoic acid, with the CAS number 125142-16-7, is a complex organic compound characterized by its branched structure and functional groups. It features a carboxylic acid group (-COOH) that imparts acidic properties, making it capable of donating protons in solution. The presence of multiple methyl groups contributes to its hydrophobic characteristics, influencing its solubility in various solvents. The compound also contains a silyl ether moiety, which enhances its stability and reactivity in organic synthesis. Its intricate stereochemistry, indicated by the specific stereocenters, suggests that it may exhibit unique biological activities or interactions. The presence of a tetrahydro-6-oxo-2H-pyran ring adds to its structural complexity, potentially affecting its reactivity and interactions with other molecules. Overall, this compound's unique combination of functional groups and stereochemistry makes it of interest in fields such as medicinal chemistry and materials science, where its properties can be exploited for various applications.
Formula:C31H54O6Si
InChI:InChI=1/C31H54O6Si/c1-11-30(7,8)28(33)36-25-16-20(2)19-31(34)15-14-21(3)24(27(25)31)13-12-22-17-23(18-26(32)35-22)37-38(9,10)29(4,5)6/h14-15,20-25,27,34H,11-13,16-19H2,1-10H3/t20-,21+,22-,23-,24+,25+,27+,31-/m1/s1
Synonyms:
  • 4-tert-Butyldimethylsilyl-4a’-hydroxy Simvastatin
  • (1S,3R,4aS,7S,8S,8aS)-8-{2-[(2R,4R)-4-{[tert-butyl(dimethyl)silyl]oxy}-6-oxotetrahydro-2H-pyran-2-yl]ethyl}-4a-hydroxy-3,7-dimethyl-1,2,3,4,4a,7,8,8a-octahydronaphthalen-1-yl 2,2-dimethylbutanoate
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