Cycloheptene TCI C0688

Chemical Identity

CAS No.: 628-92-2
PubChem: CID 12363·SID 87565775
Formula: C7H12
Molecular weight: 96.17 g/mol
Purity: >96.0%(GC)
Reference databases: ChEBI·ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: cycloheptene
SMILES: C1CCC=CCC1
InChIKey: ZXIJMRYMVAMXQP-UHFFFAOYSA-N
MDL: MDL00004156

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TCI C0688 Cycloheptene is a seven-membered cyclic alkene that serves as a versatile building block in organic synthesis. Its ring size and alkene geometry make it a useful substrate for epoxidation, hydroboration, dihydroxylation, and olefin metathesis studies. The cycloheptane framework it provides also appears in a range of natural product and pharmaceutical targets. Supplied by AMI Scientific in several package sizes, this volatile and flammable liquid should be handled in a fume hood, kept tightly closed, and stored according to the official TCI label and SDS.

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Cain et al. (2004). Conformational studies of trans-cycloheptene, trans-cycloheptene oxide, and trans-bicyclo [5.1.0] octane by ab initio calculations. Journal of Molecular Structure: THEOCHEM doi:10.1016/s0166-1280(03)00367-1
Hegab et al. (2002). Synthesis of 5-Chloro-10,11-Dihydro-5 H -Dibenzo[ a , d ]Cycloheptene-5,10-Sulfide and -5,11-Dichloro-10,11-Dihydro-5 H -Dibenzo[ A , D ]Cycloheptene-5,10-Sulfide and their Oxidation. Sulfur Letters doi:10.1080/02786110211428
Hoffmann et al. (1999). Trapped Optically Active (E)-Cycloheptene Generated by Enantiodifferentiating Z−E Photoisomerization of Cycloheptene Sensitized by Chiral Aromatic Esters. Journal of the American Chemical Society doi:10.1021/ja991315l

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