(1S)-(+)-Camphorquinone TCI C1660

Chemical Identity

Other names: (1S)-(+)-2,3-Bornanedione
CAS No.: 2767-84-2
Formula: C10H14O2
Molecular weight: 166.22 g/mol
Purity: >97.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (1S,4R)-1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione
SMILES: CC1(C2CCC1(C(=O)C2=O)C)C
InChIKey: VNQXSTWCDUXYEZ-QUBYGPBYSA-N
MDL: MDL00064159
PubChem: CID 1549179

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(1S)-(+)-Camphorquinone is a chiral compound widely used in asymmetric synthesis for the production of bioactive molecules. Its unique structure allows for the creation of compounds with specific stereochemistry, making it essential in pharmaceutical and biochemical research. This compound is particularly valuable in the development of new drugs due to its ability to form enantiomers with distinct biological activities. It is commonly used in laboratory settings for organic reactions and structural studies, especially in the field of medicinal chemistry. The compound is sensitive to oxidation and light, requiring careful handling and storage to maintain its integrity. Its role in creating complex molecular structures makes it a key component in advanced chemical research.

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(2002). CAMPHORQUINONE AND CAMPHORQUINONE MONOXIME. Organic Syntheses doi:10.15227/orgsyn.079.0125
Allonas et al. (2001). Excited-State Properties of Camphorquinone Based Monomeric and Polymeric Photoinitiators. Helvetica Chimica Acta doi:10.1002/1522-2675(20010919)84:9<2577::aid-hlca2577>3.0.co;2-q
Sionkowska et al. (1999). Comparison of the photopolymerization kinetics of triethyleneglycol dimethacrylate initiated by camphorquinone/N-phenylglycine and camphorquinone/D,L-α-phenylglycine. Polymer Bulletin doi:10.1007/s002890050621

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.