N,Nˊ-二苄基二硫代草酰胺

• 常用名: N,Nˊ-二苄基二硫代草酰胺
• 英文名: Ethanedithioamide,N1,N2-bis(phenylmethyl)
• CAS号: 122-65-6
• 分子量: 300.44200
• 密度: 1.233g/cm3
• 沸点: 451.5ºC at 760mmHg
• 分子式: C₁₆H₁₆N₂S₂
• 熔点: N/A
• 闪点: 226.8ºC

N,Nˊ-二苄基二硫代草酰胺名称

• 中文名: N,Nˊ-二苄基二硫代草酰胺
• 英文名: N,N'-dibenzylethanedithioamide

N,Nˊ-二苄基二硫代草酰胺物理化学性质

• 密度: 1.233g/cm3
• 沸点: 451.5ºC at 760mmHg
• 分子式: C₁₆H₁₆N₂S₂
• 分子量: 300.44200
• 闪点: 226.8ºC
• 精确质量: 300.07500
• PSA: 88.24000
• LogP: 4.00260
• InChIKey: KNRMURHAZMNRGD-UHFFFAOYSA-N
• SMILES: S=C(NCc1ccccc1)C(=S)NCc1ccccc1
• 蒸汽压: 2.43E-08mmHg at 25°C
• 折射率: 1.673

N,Nˊ-二苄基二硫代草酰胺毒性和生态

N,Nˊ-二苄基二硫代草酰胺安全信息

• 海关编码: 2930909090

N,Nˊ-二苄基二硫代草酰胺海关

• 海关编码: 2930909090
• 中文概述: 2930909090. 其他有机硫化合物. 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:30.0%
• 申报要素: 品名, 成分含量, 用途
• Summary: 2930909090. other organo-sulphur compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:30.0%

N,Nˊ-二苄基二硫代草酰胺靶点实验

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

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N,Nˊ-二苄基二硫代草酰胺英文别名

• EINECS 204-561-4
• Dibenzylrubeanic acid
• N,N'-Dibenzyldithiooxamide
• Dibenzylhydrorubeanic acid
• N,N'-dibenzyl-dithiooxalamide
• dibenzyldithiooxamide
• OXAMIDE,N,N'-DIBENZYLDITHIO
• USAF MK-1
• N,N'-Dibenzyl-dithiooxalamid