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CS-W001157 4
Total: USD 88.00

3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol

  • CAS No. 26021-57-8

  • Cat. No. CS-0155718
  • Purity≥98%
  • MDL No.MFCD00600394

*For research and further manufacturing use only, not for direct human use.

3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol|CS-0155718

Structure of 26021-57-8

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General Information

  • CAS No. 26021-57-8
  • Cat. No. CS-0155718
  • Purity ≥98%
  • MDL No. MFCD00600394
  • Storage 4°C, protect from light
  • Shipping Room temperature in continental US; may vary elsewhere.
  • Molecular Formula C₈H₉NO₂
  • Molecular Weight 151.16
  • Synonym(s) None
  • SMILES C1=CC2=C(C=C1O)NCCO2

Description

3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol is a bench-stable heterocyclic scaffold featuring a phenolic hydroxyl group flanked by an oxygen and nitrogen heteroatom within a fused ring system. This electron-rich framework integrates readily into medicinal chemistry campaigns targeting kinase inhibitors and CNS-active compounds. The hydroxyl moiety enables direct derivatization or hydrogen bonding interactions in binding sites.

Application

3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient access to bioactive scaffolds. Its hydroxyl group provides a handle for derivatization, while the fused oxazine ring offers structural rigidity and favorable pharmacokinetic properties. The compound exhibits good bench stability and compatibility with standard synthetic transformations, facilitating its use in late-stage functionalization and library synthesis.

Synthesis

  • Route1
    • 6-Hydroxy-2H-benzo[b][1,4]oxazin-3(4H)-one|CS-0085208
      53412-38-7
    • ~99%
    • In-stock
      3,4-Dihydro-2H-benzo[b][1,4]oxazin-6-ol|CS-0155718
      26021-57-8

    References

    • UNIVERSITY OF MASSACHUSETTS Patent: WO2009/36351 A2, 2009 ; Location in patent: Page/Page column 21; 22/24 ;
  • Route2

    References

    • Iakovou, Kriton; Kazanis, Michalis; Vavayannis, Andreas; Bruni, Giancarlo; Romeo, Maria Raffaella; Massarelli, Paola; Teramoto, Shuji; Fujiki, Hiroyuki; Mori, Toyoki European Journal of Medicinal Chemistry, 1999 , vol. 34, # 11 p. 903 - 917
  • Route3

    References

    • Iakovou, Kriton; Kazanis, Michalis; Vavayannis, Andreas; Bruni, Giancarlo; Romeo, Maria Raffaella; Massarelli, Paola; Teramoto, Shuji; Fujiki, Hiroyuki; Mori, Toyoki European Journal of Medicinal Chemistry, 1999 , vol. 34, # 11 p. 903 - 917

Safety Information

Download SDS
GHS Pictogram :
GHS No : GHS07,GHS09
Signal Word : Warning
UN#: N/A
Class : N/A
Packing Group : N/A
Hazard Statements : H302-H411
Precautionary Statements : P264-P270-P273-P301+P310-P330-P391-P501

Quality Control

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Computational Chemistry Data

  • TPSA   41.49
  • LogP   1.1965
  • H_Acceptors   3
  • H_Donors   2
  • Rotatable_Bonds   0

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