| Weight | 149.149 g/mol |
|---|---|
| Formula | C8H7NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 0 |
2H-1,4-Benzoxazin-3(4H)-one (5466-88-6)
Score:
#6643 in Chemistry
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- Hydroxamic acids derived from 2-hydroxy-2H-1,4-benzoxazin-3(4H)-one: key defense chemicals of cereals. (Journal of Agricultural and Food Chemistry, 2009)
- Decomposition of 2,4-Dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one in Aqueous Solutions. (Plant Physiology, 1978)
- Degradation Studies on Benzoxazinoids. Soil Degradation Dynamics of 2,4-Dihydroxy-7-methoxy-(2H)-1,4-benzoxazin-3(4H)-one (DIMBOA) and Its Degradation Products, Phytotoxic Allelochemicals from Gramineae (Journal of Agricultural and Food Chemistry, 2004)
- 2,4-Dihydroxy-7-methoxy-2H-1,4-benzoxazin-3(4H)-one, an Inhibitor from Zea mays with Differential Activity against Soft Rotting Erwinia Species (Plant Physiology, 1978)
- Degradation Studies on Benzoxazinoids. Soil Degradation Dynamics of (2R)-2-O-beta-D-Glucopyranosyl-4-hydroxy-(2H)-1,4-benzoxazin-3-(4H)-one (DIBOA-Glc) and Its Degradation Products, Phytotoxic Allelochemicals from Gramineae (Journal of Agricultural and Food Chemistry, 2005)
- 1,4-Benzoxazine derivatives in plants: Absence of 2,4-dihydroxy-7-methoxy-2H 1,4-benzoxazin-3/4H/-one from uninjured Zea mays plants (Phytochemistry, 1971)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(=O)NC2=CC=CC=C2O1
-
InChIKeyQRCGFTXRXYMJOS-UHFFFAOYSA-N
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