CAS: 4101-32-0; 4',5'-Dimethoxy-2'-Nitroacetophenone

该化合物是有机化合物,具有芳香结构和功能组的特点,具有两个甲基氧组和硝基组,具有化学反应和特性.乙酮的出现表明,它是一种氯酮,典型地具有碳基组(C=O)极性,可以参与各种化学反应,例如核糖化合物添加.甲基氧基组增强了苯基环的电子施食特性,有可能影响其再活性和有机溶剂中的溶解性.硝基组是电阻燃,可影响化合物的总体电子特性和再活性.由于其独特的结构特征,这种化合物可能对合成有机化学,特别是制药或农用化学的发展具有兴趣.应当观测安全性和处理预防措施,因为与硝基化合物的化合物可能具有敏感性并可能构成健康风险.

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CAS号204842-93-3 2,3,9,10-tetram... | CAS号7595-31-5 2-硝基-4,5-二甲氧基苯胺 | CAS号4101-30-8 2'-氨基-4',5'-二甲氧基苯乙酮 | CAS号3395-03-7 1,2-二甲氧基-4,5-二硝基苯 | CAS号33245-76-0 2-溴-1-(4,5-二甲氧基... | CAS号37942-55-5 (1S)-1-(2,3-dim... | CAS号4015-31-0 6,7-Dimethoxy-4...

合成工艺路线路线简述

  • 合成目标产物 1-(4,5-Dimethoxy-2-Nitro-Phenyl)-Ethanone 主要起始原料 3,4-Dimethoxyacetophenone
  • (文献来源)合成步骤主要原料 3,4-Dimethoxyacetophenone
📜香草乙酮置于硝酸,Potassium Carbonate体系中,用 丙酮 作为反应溶剂,化学反应 4.0H,反应生成 1-(4,5-二甲氧基-2-硝基苯基)乙酮
参考文献:使用异氰酸酯参与的多组分反应基于结构的新型4-(2-氟苯氧基)喹啉衍生物作为c-Met抑制剂的发现
标题:使用异氰酸酯参与的多组分反应基于结构的新型4-(2-氟苯氧基)喹啉衍生物作为c-Met抑制剂的发现
摘要:由于c-Met激酶与许多人类癌症的进展,不良的临床结果甚至耐药性密切相关,因此它已成为小分子抗肿瘤药开发的有希望的目标.在这项研究中,设计,合成和评估了两个新颖的系列的6,7-取代的4-(2-氟苯氧基)喹啉衍生物,它们包含α-酰氧基羧酰胺或α-酰氨基酰胺支架.针对c-Met激酶和四种癌细胞系(h460,Ht-29,Mkn-45和mda-Mb-231)的生物学活性.大多数目标化合物显示出中等至显着的效力,并具有对h460和ht-29癌细胞系的选择性.初步的结构活性关系表明,α-酰氧基羧酰胺或α-酰氨基酰胺作为5-原子连接体有助于抗肿瘤效力.在这些化合物中,化合物10M(c-Met Ic 50 = 2.43 Nm,多靶酪氨酸激酶抑制剂)对具有ic 50的h460,Ht-29和mda-Mb-231细胞系表现出最强的抑制活性0.14+/-0.03μm,0.20+/-0.02μm和0.42+/-0.03μm的活性分别是福瑞替尼的1
DOI:10.1016/j.Ejmech.2020.112241

海关参考信息

专利信息


专利号:US-4490374-A
优先权日:1982-09-30
标 题:5,6-Dialkoxy-3,4-optionally substituted-2(1H)quinazolinones, composition and method of use
发明人:BANDURCO VICTOR T; LEVINE SEYMOUR D; MULVEY DENNIS M; TOBIA ALFONSO J
权利人:ORTHO PHARMA CORP
摘要:The synthesis of substituted quinazolinones is described. The novel quinazolinones are renal vasodilators and thereby increase renal blood flow, and are useful as cardiovascular agents.

专利号:US-6384264-B1
优先权日:1997-12-24
标题:Photoactive materials applicable to imaging systems
发明人:DOS SANTOS CRISTIANO MARIA DE; DAVIES JOHN KYNASTON; DOWD SHARON; JOHNSTONE ROBERT ALEXANDER WAL; PRATT MICHAEL JOHN; WADE JOHN ROBERT
权利人:AGFA GEVAERT
摘要:Organic photoprecursors of amines are provided for use in photosensitive imaging systems, finding particular application in the preparation of lithographic printing plates. Said photoprecursors generate free amines on exposure to long wavelength UV or visible radiation, have high solubility in organic solvents, and include photolabile 2-nitrobenzyl functional groups. Methods for the synthesis of the photoprecursors are described, and the use of the said photoprecursors for the production of printing plates using both positive working and negative working techniques are discussed.

专利号:US-4631283-A
优先权日:1982-09-30
标 题:Ortho substituted dihydroxy-2(1H)quinazolinone-1-alkanoic acids
发明人:BANDURCO VICTOR T; LEVINE SEYMOUR D; MULVEY DENNIS M; TOBIA ALFONSO J
权利人:ORTHO PHARMA CORP
摘要:The synthesis of substituted quinazolinones is described. The novel quinazolinones are renal vasodilators and thereby increase renal blood flow, and are useful as cardiovascular agents.

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📌 第三方产品分析报告

✅ COA系统入驻 | 共享模式

主要参考文献

参考标题:Gold-Catalyzed Synthesis Of Quinolines From Propargyl Silyl Ethers And Anthranils Through The Umpolung Of A Gold Carbene Carbon
作者:Hongming Jin,Bin Tian,Xinlong Song,Jin Xie,Matthias Rudolph,Frank Rominger,A. Stephen K. Hashmi |发布日期:2016.10.4
摘要:Proceeds Through A Sequential Ring Opening/1,2‐h‐shift/protodeauration/mukaiyama Aldol Cyclization. This Method Offers A Regiospecific And Modular Access To 2‐aminoquinolines And Other Quinoline Derivatives Under Mild Conditions And With A Broad Functional‐group Tolerance. The Conversion Is Possible On A Gram Scale, Which Underlines The Synthetic Practicability Of This Methodology. The Versatility Of The

合成参考文献


参考文献:10.1007/s00424-002-0832-y
摘要:Park M, Tepikin AV, Petersen OH. What can we learn about cell signalling by combining optical imaging and patch clamp techniques Pflügers Archiv - European Journal of Physiology. 2002 Jun;444(3):305–16. doi: 10.1007/s00424-002-0832-y.
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