5-甲氧羰基-2-吡啶甲酸结构式
|
常用名 | 5-甲氧羰基-2-吡啶甲酸 | 英文名 | 5-(Methoxycarbonyl)-2-pyridinecarboxylic acid |
|---|---|---|---|---|
| CAS号 | 17874-79-2 | 分子量 | 181.145 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 347.9±27.0 °C at 760 mmHg | |
| 分子式 | C8H7NO4 | 熔点 | 187 °C | |
| MSDS | N/A | 闪点 | 164.2±23.7 °C |
| 中文名 | 5-(甲氧羰基)-2-吡啶羧酸 |
|---|---|
| 英文名 | 5-(Methoxycarbonyl)-2-pyridinecarboxylic acid |
| 中文别名 | 5-甲氧羰基-2-吡啶甲酸 | 5-(甲氧羰基)-2-吡啶甲酸 |
| 英文别名 | 更多 |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 347.9±27.0 °C at 760 mmHg |
| 熔点 | 187 °C |
| 分子式 | C8H7NO4 |
| 分子量 | 181.145 |
| 闪点 | 164.2±23.7 °C |
| 精确质量 | 181.037506 |
| PSA | 76.49000 |
| LogP | 0.49 |
| InChIKey | NTCKZTBRFXTYBD-UHFFFAOYSA-N |
| SMILES | COC(=O)c1ccc(C(=O)O)nc1 |
| 外观性状 | 固体 |
| 蒸汽压 | 0.0±0.8 mmHg at 25°C |
| 折射率 | 1.560 |
| 储存条件 | 室温, 惰性气体 |
| 分子结构 | 1、 摩尔折射率:43.04 2、 摩尔体积(m3/mol):133.0 3、 等张比容(90.2K):368.3 4、 表面张力(dyne/cm):58.7 5、 极化率(10-24cm3):17.06 |
| 计算化学 | 1.疏水参数计算参考值(XlogP):0.6 2.氢键供体数量:1 3.氢键受体数量:5 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76.5 7.重原子数量:13 8.表面电荷:0 9.复杂度:216 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:不确定 2. 密度(g/mL,25/4℃):不确定 3. 相对蒸汽密度(g/mL,空气=1):不确定 4. 熔点(ºC):187 5. 沸点(ºC,常压):不确定 6. 沸点(ºC, 5.2kPa):不确定 7. 折射率:不确定 8. 闪点(ºC):不确定 9. 比旋光度(º):不确定 10. 自燃点或引燃温度(ºC):不确定 11. 蒸气压(kPa,25ºC):不确定 12. 饱和蒸气压(kPa,60ºC):不确定 13. 燃烧热(KJ/mol):不确定 14. 临界温度(ºC):不确定 15. 临界压力(KPa):不确定 16. 油水(辛醇/水)分配系数的对数值:不确定 17. 爆炸上限(%,V/V):不确定 18. 爆炸下限(%,V/V):不确定 19. 溶解性:不确定 |
| 危害码 (欧洲) | Xn:Harmful; |
|---|---|
| 风险声明 (欧洲) | R22;R36/37/38 |
| 安全声明 (欧洲) | S26-S36/37/39-S22 |
| 海关编码 | 2933399090 |
|
~90%
5-甲氧羰基-2-吡啶甲酸 17874-79-2 |
| 文献:Oila, Markku J.; Tois, Jan E.; Koskinen, Ari M.P. Tetrahedron Letters, 2005 , vol. 46, # 6 p. 967 - 969 |
|
~%
5-甲氧羰基-2-吡啶甲酸 17874-79-2 |
| 文献:Journal of the American Chemical Society, , vol. 127, # 34 p. 11914 - 11915 |
| 海关编码 | 2933399090 |
|---|---|
| 中文概述 | 2933399090. 其他结构含非稠合吡啶环的化合物. 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 | 2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0% |
|
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
|
|
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: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
|
|
实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
|
|
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.
|
|
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: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
|
| 5-(Methoxycarbonyl)picolinic acid |
| MFCD00179343 |
| 5-methoxycarbonylpyridine-2-carboxylic acid |
| 2,5-Pyridinedicarboxylic acid, 5-methyl ester |
| 5-(Methoxycarbonyl)-2-pyridinecarboxylic acid |
| 5-(methoxycarbonyl)pyridine-2-carboxylic acid |