前往化源商城

Benzothiazole,2-(phenylmethyl)

更新时间:2025-08-22 07:00:28

Benzothiazole,2-(phenylmethyl)结构式
Benzothiazole,2-(phenylmethyl)结构式
品牌特惠专场
常用名 Benzothiazole,2-(phenylmethyl) 英文名 Benzothiazole,2-(phenylmethyl)
CAS号 6265-94-7 分子量 225.30900
密度 1.213g/cm3 沸点 374.6ºC at 760 mmHg
分子式 C14H11NS 熔点 N/A
MSDS N/A 闪点 183.6ºC

 Benzothiazole,2-(phenylmethyl)名称

英文名 2-benzyl-1,3-benzothiazole
英文别名 更多

 Benzothiazole,2-(phenylmethyl)物理化学性质

密度 1.213g/cm3
沸点 374.6ºC at 760 mmHg
分子式 C14H11NS
分子量 225.30900
闪点 183.6ºC
精确质量 225.06100
PSA 41.13000
LogP 3.88710
InChIKey MBWYZECWEVLZGI-UHFFFAOYSA-N
SMILES c1ccc(Cc2nc3ccccc3s2)cc1
折射率 1.676

 Benzothiazole,2-(phenylmethyl)合成线路

 Benzothiazole,2-(phenylmethyl)靶点实验

查看更多实验

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:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1100
实验名称:qHTS for Inhibitors of human tyrosyl-DNA phosphodiesterase 1 (TDP1): qHTS in cells in...
来源:NCGC
靶标:TDP1 protein [Homo sapiens]
External Id:TDP1101
实验名称:Schnurri-3 Inhibitors: specific inducers of adult bone formation Measured in Cell-Bas...
来源:Broad Institute
靶标:N/A
External Id:2134-01_Inhibitor_SinglePoint_HTS_Activity_Set2
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:High throughput screen for small molecule inhibitors of a hypoxia-regulated fluoresce...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:N/A
External Id:HMS1149-MLP
实验名称:qHTS for Inhibitors of AMA1-RON; Towards Development of Antimalarial Drug Lead: Prima...
来源:NCGC
靶标:apical membrane antigen 1, AMA1 [Plasmodium falciparum 3D7]
External Id:AMA1100
共96条,当前第1页,共10页
1
2
3
4
5

 Benzothiazole,2-(phenylmethyl)英文别名

2-Benzylbenzothiazol
2-benzothiazole
2-benzyl-benzothiazole
2-benzylbenzo[d]thiazole
benzothiazole,2-(phenylmethyl)
2-benzylthiazole
本网页内容来自不同专业数据源,如对内容有疑义,欢迎联系service1@chemsrc.com。