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六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓

更新时间:2025-09-10 16:07:07

六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓结构式
六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓结构式
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常用名 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓 英文名 1H-1,4-Diazepine,hexahydro-1,4-bis(phenylsulfonyl)
CAS号 5451-44-5 分子量 380.48200
密度 1.354 g/cm3 沸点 562.2ºC at 760mmHg
分子式 C17H20N2O4S2 熔点 N/A
MSDS N/A 闪点 293.8ºC

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓名称

中文名 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓
英文名 1,4-bis(benzenesulfonyl)-1,4-diazepane
中文别名 六氢-1,4-双(苯基磺酰基)-1H-1,4-二氮杂卓 | N,N-双苯磺酰二氮七环

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓物理化学性质

密度 1.354 g/cm3
沸点 562.2ºC at 760mmHg
分子式 C17H20N2O4S2
分子量 380.48200
闪点 293.8ºC
精确质量 380.08600
PSA 91.52000
LogP 3.80930
InChIKey FCGCYYIJRZRGDT-UHFFFAOYSA-N
SMILES O=S(=O)(c1ccccc1)N1CCCN(S(=O)(=O)c2ccccc2)CC1
折射率 1.614

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓安全信息

海关编码 2933990090

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓合成线路

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六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓结构式

六氢-1,4-二苯磺酰基-1H...

5451-44-5

文献:Ishiguro; Matsumura Yakugaku Zasshi, 1959 , vol. 79, p. 153,156 Chem.Abstr., 1959 , p. 13163

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六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓结构式

六氢-1,4-二苯磺酰基-1H...

5451-44-5

文献:Bleier Chemische Berichte, 1899 , vol. 32, p. 1828

~%

六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓结构式

六氢-1,4-二苯磺酰基-1H...

5451-44-5

文献:Ishiguro; Matsumura Yakugaku Zasshi, 1959 , vol. 79, p. 153,156 Chem.Abstr., 1959 , p. 13163

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓上下游产品

六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓上游产品  4

六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓下游产品  3

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓海关

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%

 六氢-1,4-二苯磺酰基-1H-1,4-二氮杂卓靶点实验

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: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:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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:Primary Screen Inhibitors of CD40 Signaling in BL2 Cells Measured in Cell-Based Syste...
来源:Broad Institute
靶标:N/A
External Id:7124-01_Inhibitor_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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