(S)-(+)-Carvone TCI C0704

Chemical Identity

Other names: (S)-(+)-p-Mentha-6,8-dien-2-one
CAS No.: 2244-16-8
PubChem: CID 16724·SID 87565789
Formula: C10H14O
Molecular weight: 150.22 g/mol
Purity: >98.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (5S)-2-methyl-5-prop-1-en-2-ylcyclohex-2-en-1-one
SMILES: CC1=CCC(CC1=O)C(=C)C
InChIKey: ULDHMXUKGWMISQ-VIFPVBQESA-N
MDL: MDL00062997

Rp 1.298.850,00

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Volume 25mL

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TCI C0704 (S)-(+)-Carvone, CAS 2244-16-8, is the S-enantiomer of carvone and carries the characteristic caraway aroma, making it a classic teaching example of chirality and olfaction. Chemically, its α,β-unsaturated ketone and isopropenyl group provide multiple handles for conjugate addition, selective reduction, and ring construction. AMI Scientific offers this TCI chiral building block in a 25 mL pack for asymmetric synthesis, natural product chemistry, and analytical method validation. Keep the bottle tightly closed in a cool, dark place and use gloves and eye protection during handling.

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SRIKRISHNA et al. (1996). ChemInform Abstract: Chiral Synthons from Carvone. Part 16. Enantioselective Synthesis of Both (+)‐ and (‐)‐Derivatives of Bicyclo(4.3.0)nonan‐8‐one and ‐3,8‐ diones from (R)‐Carvone.. ChemInform doi:10.1002/chin.199626231
Srikrishna et al. (1990). Chiral synthons from carvone. Part 4. Radical cyclization strategies to bridged systems. Synthesis of bicyclo[3.2.1]octan-3-ones from (S)-carvone. The Journal of Organic Chemistry doi:10.1021/jo00303a023
Shing et al. (2006). Total Synthesis of (‐)‐Samaderine Y from (S)‐(+)‐Carvone.. ChemInform doi:10.1002/chin.200616178

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