5-甲基-1H-吡唑-3-碳酰肼结构式
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常用名 | 5-甲基-1H-吡唑-3-碳酰肼 | 英文名 | 5-Methyl-1H-pyrazole-3-carbohydrazide |
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| CAS号 | 40535-14-6 | 分子量 | 140.14300 | |
| 密度 | 1.337g/cm3 | 沸点 | N/A | |
| 分子式 | C5H8N4O | 熔点 | 157 °C | |
| MSDS | 美版 | 闪点 | N/A | |
| 符号 |
GHS07 |
信号词 | Warning |
| 中文名 | 3-甲基-1H-吡唑-5-羧肼 |
|---|---|
| 英文名 | 5-Methyl-1H-pyrazole-3-carboxylic acid hydrazide |
| 中文别名 | 5-甲基-1-H-吡唑-3-羧肼 | 3-甲基-1H-吡唑-5-羧酸肼 | 5-甲基-2-H-吡唑-3-羧肼 |
| 英文别名 | 更多 |
| 密度 | 1.337g/cm3 |
|---|---|
| 熔点 | 157 °C |
| 分子式 | C5H8N4O |
| 分子量 | 140.14300 |
| 精确质量 | 140.07000 |
| PSA | 83.80000 |
| LogP | 0.41280 |
| InChIKey | FWNHUZOBVQZERU-UHFFFAOYSA-N |
| SMILES | Cc1cc(C(=O)NN)n[nH]1 |
| 折射率 | 1.605 |
| 储存条件 | 2-8℃ |
| 分子结构 | 1、 摩尔折射率:36.12 2、 摩尔体积(cm3/mol):104.7 3、 等张比容(90.2K):301.0 4、 表面张力(dyne/cm):68.1 5、 极化率(10-24cm3):14.32 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):-0.5 2.氢键供体数量:3 3.氢键受体数量:3 4.可旋转化学键数量:1 5.互变异构体数量:11 6.拓扑分子极性表面积83.8 7.重原子数量:10 8.表面电荷:0 9.复杂度:138 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 |
| 更多 | 1.熔点(°C):157 |
| 符号 |
GHS07 |
|---|---|
| 信号词 | Warning |
| 危害声明 | H302 |
| 危害码 (欧洲) | Xi: Irritant; |
| 风险声明 (欧洲) | R36/37/38 |
| 安全声明 (欧洲) | S26-S36/37/39 |
| 危险品运输编码 | NONH for all modes of transport |
| 海关编码 | 2933199090 |
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5-甲基-1H-吡唑-3-碳酰肼 40535-14-6 |
| 文献:Dewar; King Journal of the Chemical Society, 1945 , p. 114 Full Text Show Details Musante; Mugnaini Gazzetta Chimica Italiana, 1947 , vol. 77, p. 182,193 |
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5-甲基-1H-吡唑-3-碳酰肼 40535-14-6 |
| 文献:Musante; Mugnaini Gazzetta Chimica Italiana, 1947 , vol. 77, p. 182,193 |
|
~%
5-甲基-1H-吡唑-3-碳酰肼 40535-14-6 |
| 文献:Musante; Mugnaini Gazzetta Chimica Italiana, 1947 , vol. 77, p. 182,193 |
|
~%
5-甲基-1H-吡唑-3-碳酰肼 40535-14-6 |
| 文献:Dewar; King Journal of the Chemical Society, 1945 , p. 114 |
| 5-甲基-1H-吡唑-3-碳酰肼上游产品 4 | |
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| 5-甲基-1H-吡唑-3-碳酰肼下游产品 0 | |
| 海关编码 | 2933199090 |
|---|---|
| 中文概述 | 2933199090. 其他结构上有非稠合吡唑环化合物. 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 | 2933199090. other compounds containing an unfused pyrazole ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
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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
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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
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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
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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
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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
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实验名称:High throughput fluorescence intensity-based biochemical assay to screen for small mo...
来源:University of Pittsburgh Molecular Library Screening Center
靶标:furin (paired basic amino acid cleaving enzyme), isoform CRA_a [Homo sapiens]
External Id:MH080376 Biochemical HTS for Inhibitors of the Proprotein Convertase Furin.
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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
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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
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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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| 5-Methyl-1H-pyrazole-3-carbohydrazide |
| MFCD03423274 |