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CAS 10334-26-6

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D-(-)-Camphorquinone

Description:
D-(-)-Camphorquinone, with the CAS number 10334-26-6, is a bicyclic organic compound derived from camphor. It is characterized by its yellow crystalline appearance and is known for its distinctive camphor-like odor. This compound is a ketone, featuring a quinone structure, which contributes to its reactivity and utility in various chemical applications. D-(-)-Camphorquinone is often utilized as a photoinitiator in polymerization processes, particularly in dental materials and coatings, due to its ability to absorb UV light and initiate radical polymerization. Additionally, it exhibits interesting properties such as being a chiral molecule, which makes it valuable in asymmetric synthesis. The compound is soluble in organic solvents but has limited solubility in water. Its stability and reactivity can be influenced by environmental factors such as light and temperature, making it important to handle it under controlled conditions. Overall, D-(-)-Camphorquinone is a significant compound in both synthetic organic chemistry and industrial applications.
Formula:C10H14O2
InChI:InChI=1S/C10H14O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6H,4-5H2,1-3H3/t6-,10+/m1/s1
InChI key:InChIKey=VNQXSTWCDUXYEZ-LDWIPMOCSA-N
SMILES:C[C@@]12C(C)(C)[C@@](C(=O)C1=O)(CC2)[H]
Synonyms:
  • (-)-Camphorquinone
  • (1R)-()-Camphorquinone
  • (1R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
  • (1R)-2,3-Bornanedione
  • (1R,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
  • (1R,4S)-(-)Camphorquinone
  • (1R,4S)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
  • (1R,4S)-2,3-Bornanedione
  • 2,3-Bornanedione, (1R,4S)-(-)-
  • Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1R)-
  • See more synonyms
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