3-羧基甲基-2-氧代-2,3-二氢-1H-苯并咪唑]乙酸结构式
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常用名 | 3-羧基甲基-2-氧代-2,3-二氢-1H-苯并咪唑]乙酸 | 英文名 | 1H-Benzimidazole-1,3(2H)-diaceticacid, 2-oxo |
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| CAS号 | 1848-99-3 | 分子量 | 250.20700 | |
| 密度 | 1.548g/cm3 | 沸点 | 513.2ºC at 760mmHg | |
| 分子式 | C11H10N2O5 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 264.2ºC |
| 中文名 | 3-羧基甲基-2-氧代-2,3-二氢-1H-苯并咪唑]乙酸 |
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| 英文名 | 2-[3-(carboxymethyl)-2-oxobenzimidazol-1-yl]acetic acid |
| 英文别名 | 更多 |
| 密度 | 1.548g/cm3 |
|---|---|
| 沸点 | 513.2ºC at 760mmHg |
| 分子式 | C11H10N2O5 |
| 分子量 | 250.20700 |
| 闪点 | 264.2ºC |
| 精确质量 | 250.05900 |
| PSA | 101.53000 |
| InChIKey | JMTPLUIWGNLLNB-UHFFFAOYSA-N |
| SMILES | O=C(O)Cn1c(=O)n(CC(=O)O)c2ccccc21 |
| 蒸汽压 | 2.35E-11mmHg at 25°C |
| 海关编码 | 2933990090 |
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~76%
3-羧基甲基-2-氧代-2,3... 1848-99-3 |
| 文献:Khalikov, S. S.; Kadyrov, Ch. Sh.; Ayupova, A. T.; Molchanov, L. V. Chemistry of Heterocyclic Compounds (New York, NY, United States), 1985 , vol. 21, # 11 p. 1251 - 1254 Khimiya Geterotsiklicheskikh Soedinenii, 1985 , vol. 21, # 11 p. 1517 - 1520 |
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~%
3-羧基甲基-2-氧代-2,3... 1848-99-3 |
| 文献:Clark; Pessolano Journal of the American Chemical Society, 1958 , vol. 80, p. 1662 |
| 海关编码 | 2933990090 |
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| 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:qHTS screening for TAG (triacylglycerol) accumulators in algae
来源:11812
靶标:N/A
External Id:FATTTLab-Algae-Lipid
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实验名称:Inhibition of purified human recombinant APE1 expressed in Escherichia coli M15 cells
来源:ChEMBL
靶标:DNA-(apurinic or apyrimidinic site) endonuclease
External Id:CHEMBL1021377
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实验名称:Dicer-mediated maturation of pre-microRNA
来源:Center for Chemical Genomics, University of Michigan
靶标:N/A
External Id:TargetID_659_CEMA
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实验名称:Inhibitors of CDC25B-CDK2/CyclinA interaction
来源:Center for Chemical Genomics, University of Michigan
External Id:MScreen:TargetID_600
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实验名称:Alphascreen assay for small molecules abrogating mHTT-CaM Interaction
来源:24983
靶标:Huntingtin
External Id:KUHTS-Muma KU-CaM-Htt INH-01
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实验名称:APE1 Inhibition Assay from Article 10.1021/jm800739m: "Pharmacophore guided discovery...
来源:BindingDB
靶标:N/A
External Id:BindingDB_2983_1
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| 1.3-Bis-carboxymethyl-benzimidazolon |
| 1,3-dicarboxymethylbenzimidazolin-2-one |