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3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮

更新时间:2025-09-18 22:29:49

3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮结构式
3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮结构式
品牌特惠专场
常用名 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮 英文名 2-Propanone,3-(1H-benzimidazol-2-yl)-1,1,1-trifluoro
CAS号 782-55-8 分子量 228.17100
密度 1.444g/cm3 沸点 371.3ºC at 760 mmHg
分子式 C10H7F3N2O 熔点 N/A
MSDS N/A 闪点 178.3ºC

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮名称

中文名 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮
英文名 3-(1H-benzimidazol-2-yl)-1,1,1-trifluoropropan-2-one

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮物理化学性质

密度 1.444g/cm3
沸点 371.3ºC at 760 mmHg
分子式 C10H7F3N2O
分子量 228.17100
闪点 178.3ºC
精确质量 228.05100
PSA 45.75000
LogP 2.23680
InChIKey HJYPHXMVQPUHIO-UHFFFAOYSA-N
SMILES O=C(Cc1nc2ccccc2[nH]1)C(F)(F)F
折射率 1.562

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮安全信息

海关编码 2933990090

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮上下游产品

3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮上游产品  4

3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮下游产品  0

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮海关

海关编码 2933990090
中文概述 2933990090. 其他仅含氮杂原子的杂环化合物. 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, 乌洛托品请注明外观, 6-己内酰胺请注明外观, 签约日期
Summary 2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

 3-(1H-苯并咪唑-2-基)-1,1,1-三氟-2-丙酮靶点实验

查看更多实验

实验名称:In vitro cytotoxic activity against human salivary gland tumor (HSG) cells.
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL695228
实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
实验名称:Chemical Probes of Kaposi's Sarcoma Herpes Virus Latent Infection
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:ORF 73 [Human herpesvirus 8 type M]
External Id:HMS791
实验名称:In vitro cytotoxic activity against human gingival fibroblasts (HGF).
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL690261
实验名称:In vitro inhibitory activity evaluated against Helicobacter pylori (HP)
来源:ChEMBL
靶标:Helicobacter pylori
External Id:CHEMBL693570
实验名称:In vitro cytotoxic activity against human squamous cell carcinoma (HSC-2) cells.
来源:ChEMBL
靶标:NON-PROTEIN TARGET
External Id:CHEMBL695064
实验名称:High-throughput screen for inhibitors of the GIV GBA-motif interaction with Galpha-i ...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS1303
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
实验名称:Cell-based high throughput primary assay to identify activators of GPR151
来源:The Scripps Research Institute Molecular Screening Center
靶标:RecName: Full=G-protein coupled receptor 151; AltName: Full=G-protein coupled receptor PGR7; AltName: Full=GPCR-2037; AltName: Full=Galanin receptor 4; AltName: Full=Galanin-receptor-like protein; Short=GalRL
External Id:GPR151_PHUNTER_AG_LUMI_1536_1X%ACT
实验名称:AlphaScreen-based biochemical high throughput primary assay to identify activators of...
来源:The Scripps Research Institute Molecular Screening Center
靶标:N/A
External Id:FBW7_ACT_ALPHA_1536_1X%ACT PRUN
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