2,6-二氯-7-甲基嘌呤

• 常用名: 2,6-二氯-7-甲基嘌呤
• 英文名: 2,6-Dichloro-7-methylpurine
• CAS号: 2273-93-0
• 分子量: 203.029
• 密度: 1.8±0.1 g/cm3
• 沸点: 307.2±52.0 °C at 760 mmHg
• 分子式: C₆H₄Cl₂N₄
• 熔点: 260-262ºC
• 闪点: 139.6±30.7 °C

2,6-二氯-7-甲基嘌呤名称

• 中文名: 2,6-二氯-7-甲基嘌呤
• 英文名: 2,6-dichloro-7-methylpurine
• 中文别名: 2,6-二氯-7甲基-7H-嘌呤

2,6-二氯-7-甲基嘌呤物理化学性质

• 密度: 1.8±0.1 g/cm3
• 沸点: 307.2±52.0 °C at 760 mmHg
• 熔点: 260-262ºC
• 分子式: C₆H₄Cl₂N₄
• 分子量: 203.029
• 闪点: 139.6±30.7 °C
• 精确质量: 201.981308
• PSA: 43.60000
• LogP: 1.26
• InChIKey: HVMUWHZAZGTMJK-UHFFFAOYSA-N
• SMILES: Cn1cnc2nc(Cl)nc(Cl)c21
• 外观性状: 灰白色结晶粉末
• 蒸汽压: 0.0±0.7 mmHg at 25°C
• 折射率: 1.760
• 储存条件: 2-8°C
• 计算化学:

  1.疏水参数计算参考值（XlogP）:2

  2.氢键供体数量:0

  3.氢键受体数量:3

  4.可旋转化学键数量:0

  5.互变异构体数量:无

  6.拓扑分子极性表面积:43.6

  7.重原子数量:12

  8.表面电荷:0

  9.复杂度:179

  10.同位素原子数量:0

  11.确定原子立构中心数量:0

  12.不确定原子立构中心数量:0

  13.确定化学键立构中心数量:0

  14.不确定化学键立构中心数量:0

  15.共价键单元数量:1

2,6-二氯-7-甲基嘌呤毒性和生态

2,6-二氯-7-甲基嘌呤安全信息

• 危害码 (欧洲): Xi: Irritant;
• 风险声明 (欧洲): 22
• 海关编码: 2933990090

2,6-二氯-7-甲基嘌呤海关

• 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%

2,6-二氯-7-甲基嘌呤靶点实验

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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：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

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2,6-二氯-7-甲基嘌呤英文别名

• 2,6-Dichloro-7-methyl-7H-purine
• MFCD00039690
• 2,6-Dichlor-7-methyl-ourin
• 7H-Purine,2,6-dichloro-7-methyl
• Purine,2,6-dichloro-7-methyl
• 2,6-Dichloro-7-methylpurine
• 7-Methyl-2.6-dichlor-purin
• 2,6-dichlor-7-methyl-7h-purin