7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE
- Product Name
- 7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE
- CAS No.
- 6529-94-8
- Chemical Name
- 7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE
- Synonyms
- 7-methoxy-4H-1,4-benzoxazin-3-one;7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE;2H-1,4-Benzoxazin-3(4H)-one, 7-methoxy-;7-Methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one;7-Methoxy-3,4-dihydro-2H-1,4-benzoxazin-3-one
- CBNumber
- CB02448488
- Molecular Formula
- C9H9NO3
- Formula Weight
- 179.17
- MOL File
- 6529-94-8.mol
7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE Property
- Melting point:
- 158-160 °C(Solv: ethyl acetate (141-78-6); hexane (110-54-3))
- Boiling point:
- 374.0±42.0 °C(Predicted)
- Density
- 1.245±0.06 g/cm3(Predicted)
- storage temp.
- Sealed in dry,Room Temperature
- pka
- 12.12±0.20(Predicted)
- Appearance
- Brown to black Solid
Hazard and Precautionary Statements (GHS)
- Symbol(GHS)
-
- Signal word
- Warning
- Hazard statements
-
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
- Precautionary statements
-
P261Avoid breathing dust/fume/gas/mist/vapours/spray.
P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.
N-Bromosuccinimide Price
- Product number
- M916053
- Product name
- 7-Methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one
- Packaging
- 10mg
- Price
- $45
- Updated
- 2021/12/16
- Product number
- M916053
- Product name
- 7-Methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one
- Packaging
- 50mg
- Price
- $130
- Updated
- 2021/12/16
- Product number
- M916053
- Product name
- 7-Methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one
- Packaging
- 100mg
- Price
- $200
- Updated
- 2021/12/16
- Product number
- CHM0151403
- Product name
- 7-METHOXY-2H-BENZO(B)(1,4)OXAZIN-3(4H)-ONE
- Purity
- 95.00%
- Packaging
- 5MG
- Price
- $505.49
- Updated
- 2021/12/16
- Product number
- CM123229
- Product name
- 7-methoxy-2H-benzo[b][1,4]oxazin-3(4H)-one
- Purity
- 97%
- Packaging
- 1g
- Price
- $327
- Updated
- 2021/12/16
7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE Chemical Properties,Usage,Production
Synthesis
1268818-19-4
6529-94-8
GENERAL METHOD: 2a (2 mmol) was dissolved in acetic acid (10 mL) and powdered iron (12 mmol) was added with stirring. The reaction mixture was heated to reflux for 2 hours, during which time the progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was cooled to room temperature and concentrated under reduced pressure to remove acetic acid. Ethyl acetate (EtOAc, 20 mL) was added, stirred for 2 min and filtered to remove iron impurities. The insoluble iron residue was washed with ethyl acetate (20 mL). The filtrate and washings were combined and dried with anhydrous magnesium sulfate (MgSO4). The solvent was removed by concentration under reduced pressure and the resulting crude product was purified by column chromatography to give the pure product 3a.
References
[1] Tetrahedron, 2011, vol. 67, # 6, p. 1187 - 1192
[2] European Journal of Medicinal Chemistry, 2017, vol. 132, p. 90 - 107
7-METHOXY-2H-1,4-BENZOXAZIN-3(4H)-ONE Preparation Products And Raw materials
Raw materials
Preparation Products
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