基本信息 |
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产品名称: | 2-氟苯胺 |
CAS: | 348-54-9 |
中文同义词: | 邻氨基氟(化)苯 ; 邻氟苯胺 ; 2-氟苯胺 |
英文同义词: | 1-AMINO-2-FLUOROBENZENE ; ORTHO FLUORO ANILINE ; 2-FLUORO-BENZENAMINE ; 2-FLUOROANILINE ; 2-FLUORO-PHENYLAMINE ; O-FLUOROANILINE ; FLUOROANILINE-2 |
MDL号: | MFCD00007642 |
氢键受体数量: | 1 |
氢键供体数量: | 1 |
Smile: | c1ccc(c(c1)N)F |
InChi: | InChI=1S/C6H6FN/c7-5-3-1-2-4-6(5)8/h1-4H,8H2 |
InChiKey: | InChIKey=FTZQXOJYPFINKJ-UHFFFAOYSA-N |
性质 |
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熔点: | -29 DEG C(LIT) |
沸点: | 182-183 DEG C(LIT)/170 °C |
密度: | DENSITY: 1.151 G/ML AT 25 DEG C(LIT) |
物理性质: | FLASHPOINT: 140 DEG F FLASHPOINT: 60 DEG C REFRACTIVE INDEX: N20/D 1.544(LIT) |
注解: | BIOCHEM/PHYSIOL ACTIONS: THE METABOLISM AND EXCRETION OF THE XENOBIOTIC COMPOUND 2-FLUOROANILINE IS IMPORTANT DUE TO HUMAN EXPOSURE IN MANUFACTURING. IT IS FOUND TO BE VERY EFFICIENTLY METABOLIZED, PRIMARILY BY 4-HYDROXYLATION WITH SUBSEQUENT SULFATE OR GLUCURONIDE FORMATION. N-ACETYLATION IS ALSO OBSERVED. AT LEAST 80% OF THE DOSE IS EXCRETED IN THE URINE WITHIN 24 HR. 2-FLUOROANILINE EXERTS ITS NEPHROTOXIC EFFECT THROUGH 4-HYROXYLATION AND SUBSEQUENT P-BENZOQUINONIMINE FORMATION RIDADR: UN 2941 6.1/PG 3 UNSPSC: 41113023 WGK: 3 |
安全信息 |
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符号: | GHS02 GHS05 GHS07 |
信号词: | Danger |
危险声明: | H226,H302,H315,H318,H335 |
警示性声明: | P261,P280,P305+P351+P338 |
危害码: | Xn |
风险声明: | R:R22;R37/38 |
安全声明: | S:S26;S39 |
WGK德国: | 3 |
闪点: | 60 °C |
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