产品名称
4-(三氟甲硫基)苯酚, 98%
InChI
1S/C7H5F3OS/c8-7(9,10)12-6-3-1-5(11)2-4-6/h1-4,11H
SMILES string
Oc1ccc(SC(F)(F)F)cc1
InChI key
YYCPTWHVKSATQK-UHFFFAOYSA-N
assay
98%
form
solid
bp
77-78 °C/7 mmHg (lit.)
mp
57-60 °C (lit.)
functional group
fluoro
thioether
Application
4-（三氟甲硫基）苯酚可用于制备苯胺基衍生物，苯胺基衍生物是合成托曲珠利的重要中间体。
General description
4-（三氟甲硫基）苯酚与 NBS（N-溴代琥珀酰亚胺）、NIS（N-碘代琥珀酰亚胺）、HNO3、HNO3/H2SO4 和 4-溴苄基溴反应，得到溴代、碘代、硝基和苄代产物。
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
Synthesis of Toltrazuril.
Chinese Journal of Pharmaceuticals / Chung-kuo i yao kung yeh tsa chih, 37(3), 145-145 (2006)
Study on the synthesis of toltrazuril.
Jiang Z-L, et al.
Chemical Reagents, 28(9), 518-518 (2006)
Marjan Jereb et al.
Organic & biomolecular chemistry, 13(10), 3103-3115 (2015-01-30)
The electrophilic aromatic ring trifluoromethylthiolation of various substituted phenols was accomplished using PhNHSCF3 (N-trifluoromethylsulfanyl)aniline, (1) in the presence of BF3·Et2O (2) or triflic acid as the promoter. The functionalization was exclusively para-selective; phenols unsubstituted in both the ortho- and para
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