• Cycloheptene (CAS 628-92-2) - TCI C0688 - AMI Scientific
1 1

TCI

CAS 628-92-2

Cycloheptene TCI C0688

Cycloheptene TCI C0688
Rp 1.988.700,00
Rp 1.988.700,00
Sale Sold out
Shipping calculated at checkout.
Volume
Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 4-5 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

↓ Unduh SDS / MSDS (PDF resmi TCI)
CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

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.

—

Brand —
CAS number —
Molecular formula —
Purity —
Category —
Pack sizes —
Physical form —
Storage —

—

  • 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.

Produk Terkait