| Weight | 135.166 g/mol |
|---|---|
| Formula | C8H9NO |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
Benzomorpholine (5735-53-5)
3,4-dihydro-2H-1,4-benzoxazine · 5735-53-5
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- Synthesis and biological evaluation of new 2-(4,5-dihydro-1H-imidazol-2-yl)-3,4-dihydro-2H-1,4-benzoxazine derivatives. (Journal of Medicinal Chemistry, 2003)
- Novel potassium channel activators : Synthesis and structure-activity relationship studies of 3,4-dihydro-2H-1,4-benzoxazine derivatives (Chemical & Pharmaceutical Bulletin, 1996)
- 3,4-Dihydro-2H-1,4-benzoxazine Derivatives Combining Thrombin Inhibitory and Glycoprotein IIb/IIIa Receptor Antagonistic Activity as a Novel Class of Antithrombotic Compounds with Dual Function (Journal of Medicinal Chemistry, 2008)
- One-pot regioselective annulation toward 3,4-dihydro-3-oxo-2H-1,4-benzoxazine scaffolds under controlled microwave heating (Tetrahedron, 2006)
- Design and synthesis of 6-chloro-3,4-dihydro-4-methyl-2H-1,4-benzoxazine-8-carboxamide derivatives as potent serotonin-3 (5-HT3) receptor antagonists. (Chemical & Pharmaceutical Bulletin, 1996)
- Benzoxazines. II. Synthesis, Conformational Analysis, and Structure-Activity Relationships of 3, 4-Dihydro-2H-1, 4-benzoxazine-8-carboxamide Derivatives as Potent and Long-Acting Serotonin-3 (5-HT3) Receptor Antagonists (Chemical & Pharmaceutical Bulletin, 1996)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 3,4-dihydro-2H-1,4-benzoxazine
- 5735-53-5
-
SMILESC1COC2=CC=CC=C2N1
-
InChIKeyYRLORWPBJZEGBX-UHFFFAOYSA-N
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Safety
Alternate Names
Estimated Properties
| Boiling Point | 255.19 C | EPA T.E.S.T. |
|---|---|---|
| Boiling Point | 237.56 C | EPI Suite |
| Density | 1.08 g/cm3 | EPA T.E.S.T. |
| Flash Point | 118.23 C | EPA T.E.S.T. |
| Melting Point | 48.69 C | EPI Suite |
| Water Solubility | 2239.45 mg/L | EPA T.E.S.T. |
| Water Solubility | 5860.2 mg/L | EPI Suite |
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Synthesis
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Benzomorpholine
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