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2-甲基-1,2-苯并异噻唑-3(2H)-酮

更新时间:2025-08-25 17:23:01

2-甲基-1,2-苯并异噻唑-3(2H)-酮结构式
2-甲基-1,2-苯并异噻唑-3(2H)-酮结构式
品牌特惠专场
常用名 2-甲基-1,2-苯并异噻唑-3(2H)-酮 英文名 2-Methyl-1,2-benzothiazol-3(2H)-one
CAS号 2527-66-4 分子量 165.212
密度 1.3±0.1 g/cm3 沸点 294.3±23.0 °C at 760 mmHg
分子式 C8H7NOS 熔点 51 °C
MSDS N/A 闪点 131.8±22.6 °C

 2-甲基-1,2-苯并异噻唑-3(2H)-酮名称

中文名 2-甲基-1,2-苯并噻唑-3-酮
英文名 2-methyl-1,2-benzothiazol-3-one
中文别名 2-甲基-1,2-苯并异噻唑啉-3-酮(MBIT)
英文别名 更多

 2-甲基-1,2-苯并异噻唑-3(2H)-酮物理化学性质

密度 1.3±0.1 g/cm3
沸点 294.3±23.0 °C at 760 mmHg
熔点 51 °C
分子式 C8H7NOS
分子量 165.212
闪点 131.8±22.6 °C
精确质量 165.024841
PSA 50.24000
LogP 1.54
InChIKey RDWXSJCICPOOKO-UHFFFAOYSA-N
SMILES Cn1sc2ccccc2c1=O
外观性状 固体
蒸汽压 0.0±0.6 mmHg at 25°C
折射率 1.650
储存条件 室温,干燥,密封

 2-甲基-1,2-苯并异噻唑-3(2H)-酮安全信息

危害码 (欧洲) Xi

 2-甲基-1,2-苯并异噻唑-3(2H)-酮合成线路

 2-甲基-1,2-苯并异噻唑-3(2H)-酮靶点实验

查看更多实验

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:Luminescence-based cell-based high throughput dose response assay to identify activat...
来源:The Scripps Research Institute Molecular Screening Center
靶标:SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2, isoform CRA_a [Homo sapiens]
External Id:BRM_ACT_LUMI_1536_3XEC50 DRUN
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:Inhibition of recombinant rat MGL expressed in human HeLa cells using 2-oleoylglycero...
来源:ChEMBL
靶标:Monoglyceride lipase
External Id:CHEMBL4356492
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: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
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 2-甲基-1,2-苯并异噻唑-3(2H)-酮英文别名

2-methyl-1,2-benzisothiazol-3(2H)-one
2-Methyl-1,2-benzothiazol-3(2H)-one
MBIT
2-methyl-1,2-benzisothiazole-3(2H)-one
N-methyl-1,2-benzoisothiazol-3(2H)-one
2-methy-1-1,2-benzisolthiazol-3-(2H)-one
2-methylbenzo[d]isothiazol-3(2H)-one
2-methylbenzisothiazolin-3-one
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