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1,4,5-Thiadiazepine,2,7-dihydro-3,6-diphenyl-, 1,1-dioxide

更新时间:2026-07-14 13:30:36

1,4,5-Thiadiazepine,2,7-dihydro-3,6-diphenyl-, 1,1-dioxide结构式
1,4,5-Thiadiazepine,2,7-dihydro-3,6-diphenyl-, 1,1-dioxide结构式
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常用名 1,4,5-Thiadiazepine,2,7-dihydro-3,6-diphenyl-, 1,1-dioxide 英文名 1,4,5-Thiadiazepine,2,7-dihydro-3,6-diphenyl-, 1,1-dioxide
CAS号 14954-09-7 分子量 298.36000
密度 1.27g/cm3 沸点 503.4ºC at 760mmHg
分子式 C16H14N2O2S 熔点 N/A
MSDS N/A 闪点 258.3ºC

 名称

英文名 3,6-diphenyl-2,7-dihydro-1,4,5-thiadiazepine 1,1-dioxide
英文别名 更多

 物理化学性质

密度 1.27g/cm3
沸点 503.4ºC at 760mmHg
分子式 C16H14N2O2S
分子量 298.36000
闪点 258.3ºC
精确质量 298.07800
PSA 67.24000
LogP 2.26040
InChIKey NHZMERSIZAOIPM-UHFFFAOYSA-N
SMILES O=S1(=O)CC(c2ccccc2)=NN=C(c2ccccc2)C1
蒸汽压 9.11E-10mmHg at 25°C
折射率 1.64

 安全信息

海关编码 2933990090

 上下游产品

上游产品  1

下游产品  0

 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%

 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: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: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
实验名称:Fluorescence polarization-based biochemical high throughput primary assay to identify...
来源:The Scripps Research Institute Molecular Screening Center
靶标:abhydrolase domain-containing protein 4 isoform 1 [Mus musculus]
External Id:ABHD4_INH_FP_1536_1X%INH PRUN
实验名称:High Throughput Screen to Identify Inhibitors Targeting HIV-1 Vif-dependent Degradati...
来源:Southern Research Institute
靶标:HIV-1 Vif
External Id:HIV1-VIF_MS
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 英文别名

3,6-Diphenyl-2,7-dihydro-1,4,5-thiadiazepin-1,1-dioxyd
2,7-Dihydro-3,6-diphenyl-1,4,5-thiadiazepin-1,1-dioxid
3,6-Diphenyl-2,7-dihydro-1,4,5-thiadiazepin-1,1-dioxid
3,6-diphenyl-2,7-dihydro-1
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