385344
4-羟基-6-(三氟甲基)嘧啶
99%
别名:
6-(三氟甲基)-4-羟基嘧啶
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关于此项目
经验公式（希尔记法）:
C5H3F3N2O
化学文摘社编号:
分子量:
164.09
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
145548
Assay:
99%
产品名称
4-羟基-6-(三氟甲基)嘧啶, 99%
InChI
1S/C5H3F3N2O/c6-5(7,8)3-1-4(11)10-2-9-3/h1-2H,(H,9,10,11)
SMILES string
Oc1cc(ncn1)C(F)(F)F
InChI key
LVOYSBZJJWPUBD-UHFFFAOYSA-N
assay
99%
mp
169-171 °C (lit.)
functional group
fluoro
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Application
4-Hydroxy-6-(trifluoromethyl)pyrimidine (6-(Trifluoromethyl)-4-pyrimidinol) may be used in the synthesis of 10-[3-(6-trifluoromethyl-pyrimidin-4-yloxy)-propoxy]-(20S)-camptothecin.
General description
4-Hydroxy-6-(trifluoromethyl)pyrimidine, a pyrimidine derivative, is a heterocyclic building block.
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
Qingyong Li et al.
Bioorganic & medicinal chemistry, 14(21), 7175-7182 (2006-07-28)
In an attempt to improve the antitumor activity and decrease the cytotoxicity of camptothecin, 18 new 10-substituted camptothecin derivatives were prepared. The cytotoxicity in vitro on cancer cell lines and antitumor activity in vivo, and inhibitory properties of topoisomerase I
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