Skip to main content

Dihydrohaplamine

  • Reference work entry
Natural Compounds

Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Quinoline Alkaloids

Biological sources: Haplophyllum perforatum

C15H17NO3: 259.1110

Mp: 231–233°C (dec., Me2CO) [1, 2]

UV: 216, 232, 278, 287, 334 [2]

IR: 3150, 1650, 1604, 1503, 1480, 1460, 1420, 1370, 1315, 1220, 1170, 1120, 1040, 860, 820, 770, 715 [1]

MS m/z: 259(M+, 100), 216(45), 204(65), 203(71), 188(28), 168(25) [1]

1 H NMR: 1.18(6H, s, 2 × CH3), 1.68(2H, t, J = 6.5, β-CH2), 2.47(2H, t, J = 6.5, γ-CH2), 3.60(3H, s, OCH3), 7.00–7.34(3H, m, H-5, 7, 8) [2]

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 549.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Hardcover Book
USD 549.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  1. V.I. Akhmedzhanova, Chem. Nat. Comp. 35, 552 (1999)

    CAS  Google Scholar 

  2. V.I. Akhmedzhanova, I.A. Bessonova, S.Yu. Yunusov, Chem. Nat. Comp. 12, 282 (1976)

    Google Scholar 

Download references

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2013 Springer Science+Business Media New York

About this entry

Cite this entry

(2013). Dihydrohaplamine. In: Azimova, S.S., Yunusov, M.S. (eds) Natural Compounds. Springer, New York, NY. https://doi.org/10.1007/978-1-4614-0560-3_1121

Download citation

Publish with us

Policies and ethics