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CAS 560-09-8

:

(1S,3R)-1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid

Description:
(1S,3R)-1,2,2-Trimethyl-1,3-cyclopentanedicarboxylic acid, with CAS number 560-09-8, is a bicyclic organic compound characterized by its unique structure featuring a cyclopentane ring with two carboxylic acid functional groups and three methyl substituents. This compound exhibits chirality, with specific stereochemistry at the 1 and 3 positions, which influences its reactivity and interactions in chemical processes. It is typically a solid at room temperature and is soluble in polar solvents due to the presence of carboxylic acid groups. The compound is of interest in organic synthesis and may serve as a building block in the production of more complex molecules. Its derivatives can be utilized in various applications, including pharmaceuticals and agrochemicals. The presence of multiple functional groups allows for diverse chemical reactivity, making it a valuable compound in synthetic organic chemistry. Safety data should be consulted for handling, as with all chemical substances, to ensure proper precautions are taken.
Formula:C10H16O4
InChI:InChI=1S/C10H16O4/c1-9(2)6(7(11)12)4-5-10(9,3)8(13)14/h6H,4-5H2,1-3H3,(H,11,12)(H,13,14)/t6-,10+/m0/s1
InChI key:InChIKey=LSPHULWDVZXLIL-QUBYGPBYSA-N
SMILES:C(O)(=O)[C@]1(C)C(C)(C)[C@H](C(O)=O)CC1
Synonyms:
  • (-)-cis-Camphoric acid
  • (1S,3R)-()-Camphoric acid
  • (1S,3R)-1,2,2-Trimethyl-1,3-Cyclopentanedicarboxylic Acid
  • (1S,3R)-1,2,2-trimethylcyclopentane-1,3-dicarboxylic acid
  • 1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, (1S,3R)-
  • 1,3-Cyclopentanedicarboxylic acid, 1,2,2-trimethyl-, (1S-cis)-
  • <span class="text-smallcaps">L</span>-Camphoric acid
  • Camphoric acid, cis-(-)-
  • l-Camphoric acid
  • ()-Camphoric acid
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