| Identification | Back Directory | [Name]
5-CHLORO-1-METHYL-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE | [CAS]
40707-01-5 | [Synonyms]
LAQU-006 5-chloro-1-methyl-3,1-benzoxazine-2,4-dione 5-CHLORO-1-METHYL-1H-BENZO[D][1,3]OXAZINE-2,4-DIONE 2H-3,1-Benzoxazine-2,4(1H)-dione, 5-chloro-1-Methyl- 5-chloro-1-Methyl-2H-benzo[d][1,3]oxazine-2,4(1H)-dione | [Molecular Formula]
C9H6ClNO3 | [MDL Number]
MFCD00047630 | [MOL File]
40707-01-5.mol | [Molecular Weight]
211.6 |
| Chemical Properties | Back Directory | [Melting point ]
217.9-218.2 °C | [Boiling point ]
344.8±44.0 °C(Predicted) | [density ]
1.476±0.06 g/cm3(Predicted) | [storage temp. ]
under inert gas (nitrogen or Argon) at 2-8°C | [pka]
-3.48±0.20(Predicted) | [Appearance]
Light brown to brown Solid | [InChI]
InChI=1S/C9H6ClNO3/c1-11-6-4-2-3-5(10)7(6)8(12)14-9(11)13/h2-4H,1H3 | [InChIKey]
BTNWNXWHFWYONH-UHFFFAOYSA-N | [SMILES]
N1(C)C2=CC=CC(Cl)=C2C(=O)OC1=O |
| Hazard Information | Back Directory | [Synthesis]
General procedure for the synthesis of 5-chloro-1-methyl-1H-benzo[d][1,3]oxazine-2,4-diones from 5-chloro-1H-benzo[d][1,3]oxazine-2,4-diones and iodomethane: Iodomethane (2 mL, 4.6 mmol, 4 equiv) and N,N-diisopropylethylamine (DIPEA, 1 mL, 0.74 mol) were suspended at room temperature in N,N-dimethylacetamide (DMA, 10 mL) and stirred for 10 min. Subsequently, 5-chloroisatoic anhydride (200 mg, 1.01 mmol, 1 eq.) was added and the reaction mixture was stirred at 40 °C for 5 hours. Upon completion of the reaction, the resulting product 5-chloro-1-methyl-1H-benzo[d][1,3]oxazine-2,4-dione was collected by filtration and washed with distilled water to give the pure product (150 mg, 70% yield). The melting point of the product was 224 °C. Infrared spectra (KBr) showed characteristic absorption peaks υ1774, 1716, 1593 cm^-1. 1H NMR (DMSO-d6, 300 MHz) δ 7.78 (t, J = 8.1 Hz, 1H), 7.42 (m, 2H), 3.45 (s, 3H). Elemental analysis results: calculated values for C9H6ClNO3: C, 51.08; H, 2.86; Cl, 16.75; N, 6.62; O, 22.68. measured values: C, 51.12; H, 2.36; Cl, 16.71; N, 6.58. | [References]
[1] Organic Process Research and Development, 2007, vol. 11, # 4, p. 674 - 680 [2] Journal of Heterocyclic Chemistry, 2016, vol. 53, # 2, p. 437 - 440 [3] European Journal of Medicinal Chemistry, 2011, vol. 46, # 1, p. 1 - 10 [4] Monatshefte fur Chemie, 2016, vol. 147, # 6, p. 1069 - 1079 [5] Journal of Medicinal Chemistry, 2004, vol. 47, # 8, p. 2075 - 2088 |
|
| Company Name: |
3A Chemicals
|
| Tel: |
400-668-9898 |
| Website: |
www.3achem.com |
|