1-(2-硝基苄基)吡咯-2-甲醛结构式
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常用名 | 1-(2-硝基苄基)吡咯-2-甲醛 | 英文名 | 1-(2-Nitrobenzyl)-1H-pyrrole-2-carbaldehyde |
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| CAS号 | 22162-51-2 | 分子量 | 230.219 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 389.8±22.0 °C at 760 mmHg | |
| 分子式 | C12H10N2O3 | 熔点 | 137-139°C | |
| MSDS | N/A | 闪点 | 189.5±22.3 °C |
1-(2-硝基苄基)吡咯-2-甲醛用途 |
| 中文名 | 1-(2-硝基苄基)吡咯-2-甲醛 |
|---|---|
| 英文名 | 1-[(2-nitrophenyl)methyl]pyrrole-2-carbaldehyde |
| 中文别名 | 1-(2-硝基苯基甲基)-2-吡咯甲醛 |
| 英文别名 | 更多 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 389.8±22.0 °C at 760 mmHg |
| 熔点 | 137-139°C |
| 分子式 | C12H10N2O3 |
| 分子量 | 230.219 |
| 闪点 | 189.5±22.3 °C |
| 精确质量 | 230.069138 |
| PSA | 67.82000 |
| LogP | 1.50 |
| InChIKey | AKFAPUIPEQSHJL-UHFFFAOYSA-N |
| SMILES | O=Cc1cccn1Cc1ccccc1[N+](=O)[O-] |
| 蒸汽压 | 0.0±0.9 mmHg at 25°C |
| 折射率 | 1.610 |
| 储存条件 | |
| 稳定性 | |
| 分子结构 | 1、 摩尔折射率:63.21 2、 摩尔体积(cm3/mol):182.2 3、 等张比容(90.2K):493.3 4、 表面张力(dyne/cm):53.7 5、 极化率(10-24cm3):25.06 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):1.9 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:3 5.互变异构体数量:无 6.拓扑分子极性表面积67.8 7.重原子数量:17 8.表面电荷:0 9.复杂度:290 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.性状:未确定 2.密度(g/mL,25/4℃):未确定 3.相对蒸汽密度(g/mL,空气=1):未确定 4.熔点(ºC):137-139 5.沸点(ºC,常压):未确定 6.沸点(ºC,5.2kPa):未确定 7.折射率:未确定 8.闪点(ºC):未确定 9.比旋光度(º):未确定 10.自燃点或引燃温度(ºC):未确定 11.蒸气压(kPa,25ºC):未确定 12.饱和蒸气压(kPa,60ºC):未确定 13.燃烧热(KJ/mol):未确定 14.临界温度(ºC):未确定 15.临界压力(KPa):未确定 16.油水(辛醇/水)分配系数的对数值:未确定 17.爆炸上限(%,V/V):未确定 18.爆炸下限(%,V/V):未确定 19.溶解性:未确定 |
| 安全声明 (欧洲) | S22-S24/25 |
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| 海关编码 | 2933990090 |
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1-(2-硝基苄基)吡咯-2-甲醛 22162-51-2 |
| 文献:REDX PHARMA LIMITED; CRAIGHEAD, Mark; PALIN, Ronald; MURRAY, Neil; LINDSAY, Derek Patent: WO2012/63085 A2, 2012 ; Location in patent: Page/Page column 90 ; WO 2012/063085 A2 |
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1-(2-硝基苄基)吡咯-2-甲醛 22162-51-2 |
| 文献:American Home Products Corporation Patent: US5521173 A1, 1996 ; US 5521173 A |
| 1-(2-硝基苄基)吡咯-2-甲醛上游产品 3 | |
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| 1-(2-硝基苄基)吡咯-2-甲醛下游产品 1 | |
| 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% |
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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...
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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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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:RecName: Full=Sialate O-acetylesterase; AltName: Full=H-Lse; AltName: Full=Sialic acid-specific 9-O-acetylesterase; Flags: Precursor [Homo sapiens]
External Id:SIAE_INH_FP_1536_1X%INH PRUN
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| 1-(2-Nitrobenzyl)-1H-pyrrole-2-carbaldehyde |
| MFCD00792865 |
| 1-(2-nitro-benzyl)-pyrrole-2-carbaldehyde |
| 1-(2-Nitro-benzyl)-pyrrol-2-carbaldehyd |
| 1-(2-Nitrobenzyl)-2-pyrrolecarboxaldehyde |