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2-(4-BROMO-PHENYL)-BENZO[D]IMIDAZO[2,1-B]THIAZOLE

更新时间:2025-10-18 15:43:17

2-(4-BROMO-PHENYL)-BENZO[D]IMIDAZO[2,1-B]THIAZOLE结构式
2-(4-BROMO-PHENYL)-BENZO[D]IMIDAZO[2,1-B]THIAZOLE结构式
品牌特惠专场
常用名 2-(4-BROMO-PHENYL)-BENZO[D]IMIDAZO[2,1-B]THIAZOLE 英文名 2-(4-BROMO-PHENYL)-BENZO[D]IMIDAZO[2,1-B]THIAZOLE
CAS号 7025-33-4 分子量 329.21400
密度 N/A 沸点 N/A
分子式 C15H9BrN2S 熔点 N/A
MSDS N/A 闪点 N/A

 名称

英文名 2-(4-Bromophenyl)imidazo[2,1-b][1,3]benzothiazole
英文别名 更多

 物理化学性质

分子式 C15H9BrN2S
分子量 329.21400
精确质量 327.96700
PSA 45.54000
LogP 4.97850
InChIKey KEPQCZGPWRNPCZ-UHFFFAOYSA-N
SMILES Brc1ccc(-c2cn3c(n2)sc2ccccc23)cc1

 安全信息

海关编码 2934100090

 上下游产品

上游产品  2

下游产品  0

 海关

海关编码 2934100090
中文概述 2934100090. 结构上含有一个非稠合噻唑环的化合物(不论是否氢化). 增值税率:17.0%. 退税率:9.0%. 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 2934100090 other compounds containing an unfused thiazole ring (whether or not hydrogenated) in the structure VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:20.0%

 靶点实验

查看更多实验

实验名称:Significant suppressive activity of delayed type hypersensitivity (DTH) with out inhi...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL720298
实验名称:Significant suppressive activity of delayed type hypersensitivity (DTH) with out inhi...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL720297
实验名称:Transrepression of GCR (unknown origin) expressed in human fibrosarcoma cells assesse...
来源:ChEMBL
靶标:Glucocorticoid receptor
External Id:CHEMBL4256402
实验名称:Significant suppressive activity of delayed type hypersensitivity (DTH) with out inhi...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL724353
实验名称:Significant suppressive activity of delayed type hypersensitivity (DTH) with out inhi...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL723679
实验名称:Antiproliferative activity against human IGROV1 cells after 72 hrs by cell counter
来源:ChEMBL
靶标:IGROV-1
External Id:CHEMBL1685947
实验名称:Transactivation of GCR (unknown origin) expressed in human fibrosarcoma cells at 0.1 ...
来源:ChEMBL
靶标:Glucocorticoid receptor
External Id:CHEMBL4256401
实验名称:Reduction of paclitaxel-induced p21 expression in human IGROV1 cells at 0.12 uM after...
来源:ChEMBL
靶标:IGROV-1
External Id:CHEMBL1685948
实验名称:Reduction of paclitaxel-induced p21 expression in human IGROV1 cells at 5 uM after 24...
来源:ChEMBL
靶标:IGROV-1
External Id:CHEMBL1685949
实验名称:Reduction of paclitaxel-induced p21 expression in human IGROV1 cells at 0.3 uM after ...
来源:ChEMBL
靶标:IGROV-1
External Id:CHEMBL1685950
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 英文别名

2-(4-bromophenyl)-4H-benzo[d][1,3]oxazin-4-one
2-phenyl-4H-3,1-benzox-azin-4-one
2-(4-Bromophenyl)benzo[d][1,3]oxazin-4-one
2-<4-Brom-phenyl>-imidazo<2,1-b>benzthiazol
2-(4-Brom-phenyl)-benz[d][1,3]oxazin-4-on
2-(4-bromo-phenyl)-benzo[d]imidazo[2,1-b]thiazole
2-(4-bromo-phenyl)-benz[d][1,3]oxazin-4-one
2-(4-bromophenyl)imidazo[2,1-b]benzothiazole
2-(p-Brom-phenyl)imidazo<2,1-b>benzothiazol
2-(4-Bromophenyl)-4H-3,1-benzoxazin-4-one
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