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4-氯苯基-2-(4-氯苯基)-1,3-噻唑

更新时间:2025-08-26 22:20:51

4-氯苯基-2-(4-氯苯基)-1,3-噻唑结构式
4-氯苯基-2-(4-氯苯基)-1,3-噻唑结构式
品牌特惠专场
常用名 4-氯苯基-2-(4-氯苯基)-1,3-噻唑 英文名 4-(chloromethyl)-2-(4-chlorophenyl)-1,3-thiazole
CAS号 17969-22-1 分子量 244.14000
密度 1.378 g/cm3 沸点 374ºC at 760 mmHg
分子式 C10H7Cl2NS 熔点 78ºC
MSDS N/A 闪点 180ºC

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑名称

中文名 4-氯苯基-2-(4-氯苯基)-1,3-噻唑
英文名 4-(chloromethyl)-2-(4-chlorophenyl)-1,3-thiazole
英文别名 更多

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑物理化学性质

密度 1.378 g/cm3
沸点 374ºC at 760 mmHg
熔点 78ºC
分子式 C10H7Cl2NS
分子量 244.14000
闪点 180ºC
精确质量 242.96800
PSA 41.13000
LogP 4.20230
InChIKey UEJQTBKTWJQBRN-UHFFFAOYSA-N
SMILES ClCc1csc(-c2ccc(Cl)cc2)n1
蒸汽压 1.85E-05mmHg at 25°C
折射率 1.617
储存条件 室温

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑MSDS

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑安全信息

危害码 (欧洲) Xi: Irritant;
风险声明 (欧洲) R36/37/38
安全声明 (欧洲) 26-36/37/39
海关编码 2934100090

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑合成线路

~78%

4-氯苯基-2-(4-氯苯基)-1,3-噻唑结构式

4-氯苯基-2-(4-氯苯基)...

17969-22-1

文献:Chemical Biology and Drug Design, , vol. 78, # 5 p. 844 - 852

~%

4-氯苯基-2-(4-氯苯基)-1,3-噻唑结构式

4-氯苯基-2-(4-氯苯基)...

17969-22-1

文献:Archiv der Pharmazie, , vol. 343, # 7 p. 411 - 416

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑上下游产品

4-氯苯基-2-(4-氯苯基)-1,3-噻唑上游产品  3

4-氯苯基-2-(4-氯苯基)-1,3-噻唑下游产品  3

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑海关

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%

 4-氯苯基-2-(4-氯苯基)-1,3-噻唑靶点实验

查看更多实验

实验名称:Primary cell-based high-throughput screening assay for identification of compounds th...
来源:Johns Hopkins Ion Channel Center
靶标:regulator of G-protein signaling 4 isoform 2 [Homo sapiens]
External Id:JHICC_RGS_Act_HTS
实验名称:Late stage assay provider results from the probe development effort to identify inhib...
来源:The Scripps Research Institute Molecular Screening Center
靶标:glutathione S-transferase omega-1 isoform 1 [Homo sapiens]
External Id:GSTO1_INH_FLUO_ABPP_1XINH_RECOMB
实验名称:Luminescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:mu-type opioid receptor isoform MOR-1 [Homo sapiens]
External Id:OPRM1-OPRD1_AG_LUMI_1536_1X%ACT PRUN
实验名称:QFRET-based biochemical primary high throughput screening assay to identify exosite i...
来源:The Scripps Research Institute Molecular Screening Center
靶标:disintegrin and metalloproteinase domain-containing protein 17 preproprotein [Homo sapiens]
External Id:ADAM17_INH_QFRET_1536_1X%INH PRUN
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify ago...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_AG_FLUO8_1536_1X%ACT PRUN
实验名称:uHTS identification of small molecule activators of the adaptive arm of the Unfolded ...
来源:Burnham Center for Chemical Genomics
靶标:N/A
External Id:BCCG-A405-UPR-XBP1-PrimaryAgonist-Assay
实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
实验名称:Fluorescence polarization to screen for inhibitor that competite the binding of FadD2...
来源:Broad Institute
靶标:FATTY-ACID-CoA LIGASE FADD28 (FATTY-ACID-CoA SYNTHETASE)
External Id:2147-01_Inhibitor_SinglePoint_HTS_Activity
实验名称:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfect...
来源:Broad Institute
靶标:N/A
External Id:Bursicon-induced LGR2 mediated cAMP production in LGR-2/CRE6x-Luciferase co-transfected HEK293 cells Inhibition - 7011-01_Antagonist_SinglePoint_HTS_Activity
实验名称:Fluorescence-based cell-based primary high throughput screening assay to identify pos...
来源:The Scripps Research Institute Molecular Screening Center
靶标:muscarinic acetylcholine receptor M1 [Homo sapiens]
External Id:CHRM1_PAM_FLUO8_1536_1X%ACT PRUN
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 4-氯苯基-2-(4-氯苯基)-1,3-噻唑英文别名

f2145-0261
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