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6-氟-2H-1,4-苯并噁唑-3(4H)-酮

6-氟-2H-1,4-苯并噁唑-3(4H)-酮名称

[ CAS 号 ]:
398-63-0

[ 中文名 ]:
6-氟-2H-1,4-苯并嗪-3(4H)-酮

[ 英文名 ]:
6-Fluoro-2H-1,4-benzoxazin-3(4H)-one

[中文别名 ]:

6-氟-2H-1,4-苯并噁唑-3(4H)-酮

[英文别名 ]:

MFCD03424565
6-Fluoro-2H-1,4-benzoxazin-3(4H)-one
6-fluoro-2,4-dihydro-1,4-benzoxazin-3-one
2H-1,4-Benzoxazin-3(4H)-one, 6-fluoro-

6-氟-2H-1,4-苯并噁唑-3(4H)-酮物理化学性质

[ 密度 ]:
1.3±0.1 g/cm3

[ 沸点 ]:
322.9±42.0 °C at 760 mmHg

[ 熔点 ]:
207-211ºC(lit.)

[ 分子式 ]:
C₈H₆FNO₂

[ 分子量 ]:
167.137

[ 闪点 ]:
149.1±27.9 °C

[ 精确质量 ]:
167.038254

[ PSA ]:
38.33000

[ LogP ]:
1.09

[ 蒸汽压 ]:
0.0±0.7 mmHg at 25°C

[ 折射率 ]:
1.540

[ 储存条件 ]:
室温

6-氟-2H-1,4-苯并噁唑-3(4H)-酮MSDS

6-氟-2H-1,4-苯并噁唑-3(4H)-酮安全信息

[ 符号 ]:

GHS07

[ 信号词 ]:
Warning

[ 危害声明 ]:
H315-H319-H335

[ 警示性声明 ]:
P261-P305 + P351 + P338

[ 个人防护装备 ]:
dust mask type N95 (US);Eyeshields;Gloves

[ 危害码 (欧洲) ]:
Xi

[ 风险声明 (欧洲) ]:
R36/37/38

[ 安全声明 (欧洲) ]:
S26-S36

[ 危险品运输编码 ]:
NONH for all modes of transport

[ 海关编码 ]:
2934999090

6-氟-2H-1,4-苯并噁唑-3(4H)-酮合成路线

6-氟-2H-1,4-苯并噁唑-3(4H)-酮上下游产品

6-氟-2H-1,4-苯并噁唑-3(4H)-酮上游产品

6-氟-2H-1,4-苯并噁唑-3(4H)-酮下游产品

6-氟-2H-1,4-苯并噁唑-3(4H)-酮海关

[ 海关编码 ]: 2934999090

[ 中文概述 ]:
2934999090. 其他杂环化合物. 增值税率:17.0%. 退税率:13.0%. 监管条件:无. 最惠国关税:6.5%. 普通关税:20.0%

[ 申报要素 ]: 品名, 成分含量, 用途

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

6-氟-2H-1,4-苯并噁唑-3(4H)-酮文献

New herbicide models from benzoxazinones: aromatic ring functionalization effects.

J. Agric. Food Chem. 54(26) , 9843-51, (2006)

The utility of benzoxazinones and some of their synthetic derivatives in the search for new leads for herbicide model development has been widely discussed. As the benzoxazinone skeleton contains thre...

Peroxidase-catalyzed halide ion oxidation.

Redox Rep. 5(4) , 169-71, (2000)

The first complete mechanistic analysis of halide ion oxidation by a peroxidase was that of iodide oxidation by horseradish peroxidase. It was shown conclusively that a two-electron oxidation of iodid...

The proximate coupling constant, 5 J (H, CH3), and the torsional mobility of the thiomethyl group in some thioanisole derivatives. Schaefer T, et al.

Can. J. Chem. 69(4) , 620-624, (1991)

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