2-甲基吲哚-3-乙酸结构式
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常用名 | 2-甲基吲哚-3-乙酸 | 英文名 | (2-Methyl-1H-indol-3-yl)acetic acid |
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| CAS号 | 1912-43-2 | 分子量 | 189.210 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 418.2±30.0 °C at 760 mmHg | |
| 分子式 | C11H11NO2 | 熔点 | 205 °C (dec.)(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 206.7±24.6 °C |
| 中文名 | 2-甲基吲哚-3-乙酸 |
|---|---|
| 英文名 | 2-(2-methyl-1H-indol-3-yl)acetic acid |
| 中文别名 | 2-甲基-3-吲哚乙酸 |
| 英文别名 | 更多 |
| 密度 | 1.3±0.1 g/cm3 |
|---|---|
| 沸点 | 418.2±30.0 °C at 760 mmHg |
| 熔点 | 205 °C (dec.)(lit.) |
| 分子式 | C11H11NO2 |
| 分子量 | 189.210 |
| 闪点 | 206.7±24.6 °C |
| 精确质量 | 189.078979 |
| PSA | 53.09000 |
| LogP | 1.89 |
| InChIKey | QJNNHJVSQUUHHE-UHFFFAOYSA-N |
| SMILES | Cc1[nH]c2ccccc2c1CC(=O)O |
| 蒸汽压 | 0.0±1.0 mmHg at 25°C |
| 折射率 | 1.671 |
| 储存条件 | 保持贮藏器密封、储存在阴凉、干燥的地方,确保工作间有良好的通风或排气装置 |
| 稳定性 | 如果遵照规格使用和储存则不会分解,未有已知危险反应,避免氧化物 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):1.9 2.氢键供体数量:2 3.氢键受体数量:2 4.可旋转化学键数量:2 5.互变异构体数量:无 6.拓扑分子极性表面积53.1 7.重原子数量:14 8.表面电荷:0 9.复杂度:229 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:固体 2. 密度(g/mL,20ºC):未确定 3. 相对蒸汽密度(g/mL,空气=1):未确定 4. 熔点(ºC):198-204 5. 沸点(ºC):未确定 6. 沸点(ºC,20mmHg):未确定 7. 折射率:未确定 8. 闪点(°C):未确定 9. 比旋光度(ºF):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,40ºC):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 |
| 个人防护装备 | Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter |
|---|---|
| 危害码 (欧洲) | Xi: Irritant; |
| 安全声明 (欧洲) | S22-S24/25 |
| 危险品运输编码 | NONH for all modes of transport |
| WGK德国 | 3 |
| 海关编码 | 2933990090 |
| 2-甲基吲哚-3-乙酸上游产品 0 | |
|---|---|
| 2-甲基吲哚-3-乙酸下游产品 10 | |
| 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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On the Mechanism of Action of Growth Regulators.
Plant Physiol. 28(2) , 218-32, (1953)
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Advances in the catalytic production of valuable levulinic acid derivatives. Zhang J, et al.
ChemCatChem 4(9) , 1230-37, (2012)
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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: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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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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| 2-METHYLINDOLE-3-ACETIC ACID |
| (2-Methyl-indol-3-yl)-essigsaeure |
| 2-Methyl-3-indoleacetic acid |
| 2-(2-methylindol-3-yl)acetic acid |
| 2-methyl-1H-indole-3-acetic acid |
| (2-methylindol-3yl)acetic acid |
| MFCD00075006 |
| (2-Methyl-1H-indol-3-yl)acetic acid |