CAS: 2441-46-5; 1,2,4,5-Tetramethoxybenzene
该化合物是属于甲氧代苯类的有机化合物,其特征为苯环,附于1,2,4,4和5个位置的四类甲氧(-OCH3),显著影响其化学特性.该化合物在室内温度下一般是无色的,可粉色黄色固体,以其芳香特性为名.多种甲氧基组的存在,增强了其在有机溶剂中的溶解性,同时影响其再活动,使其与非代苯相比,其电子嗜好度降低. 1,2,4,5-乙氧苯可参与各种化学反应,包括电益替代和氧化.尽管甲氧基苯组可以引导其再活性并影响产品的形成.此外,该化合物在有机合成和材料科学中可能具有有趣的光学特性和潜在应用.应当参考安全数据,以便处理,与所有化学物质一样,确保采取适当的预防措施.
- 英文名称1,2,4,5-Tetramethoxybenzene
- 中文名称1,2,4,5-四甲氧基苯
- IUPAC名称1,2,4,5-tetramethoxybenzene
- 其它别名Asarol Methyl Ether; Benzene, 1,2,4,5-Tetramethoxy-; 1,2,4,5-Tetramethoxybenzene
- CAS编号2441-46-5
- MFCD编号:MFCD00094450
- 分子式:C10H14O4分子量:198.22
- 产品CID: 1191744
- 产品分类有机原料→分子砌块→芳环类化合物→苯类化合物
- 相似结构搜索
- 产品信息参考
;; - InChIKey: JUVJUCAKSWHQEE-UHFFFAOYSA-N
- InChI=1S/C10H14O4/c1-11-7-5-9(13-3)10(14-4)6-8(7)12-2/h5-6H,1-4H3
- 计算化学: 氢键受体数4.0氢键供体数*可旋转键数4.0
物理性质
MSDS等安全信息
上下游产品
2-methoxy-4,5-di-acetoxyphenyl acetate 2,5-dimethoxyquinone 2,5-dimethoxyhydroquinone methyl iodide 2,3,5,6-tetramethoxybenzyl chloride 2,5-dimethoxyquinone 1,4-bis-(α-hydroxy-benzhydryl)-2,3,5,6-tetramethoxy-benzene 4-(2,3,5,6-tetramethoxy-benzyl)-morpholine合成工艺路线路线简述
📜2-甲氧基对苯二酚置于硫酸,Magnesium Sulfate,Lead Dioxide,苯体系中,化学反应生成1,2,4,5-四甲氧基苯
参考文献:Erdtman,Svensk Kemisk Tidskrift,1932,Vol. 44,P. 135,143,147
标题:Erdtman,Svensk Kemisk Tidskrift,1932,Vol. 44,P. 135,143,147
海关参考信息
- 2905110000-甲醇
2907210001-间苯二酚
2907221000-对苯二酚
2908199090-其他酚的卤化衍生物 - 💡 提示：海关信息按照顺序优先匹配，如需确认的海关信息，请参考相关资料。
- 详情请参考：📖 海关编码查询和海关进出口税则
专利信息
专利号:CN-110526811-A
优先权日:2019-09-20
标题 :A kind of α-glucosidase inhibitor and its synthesis method and application
供应商参考报价(招募中)
品牌试剂参考报价(招募中)
📌 第三方产品分析报告
主要参考文献
参考标题:Synthesis Of Polyhydroxylated Flavonoids Bearing A Lipophilic Decyl Tail As Potential Therapeutic Antioxidants作者:Stuart T. Caldwell,Donald B. Mcphail,Garry G. Duthie,Richard C. Hartley |发布日期:2012.1
摘要:Antioxidants Have Potential For The Treatment Of Stroke And Neurodegeneration, And Chimeric Compounds That Combine A Flavon-3-Ol Head Group Related To Myricetin And A Lipophilic Decyl Tail Are Known To Protect Membranes From Oxidative Damage At Least As Well As Vitamin E. New Flavon-3-Ols That Are Highly Hydroxylated In The B Ring In Ways Not Found In Natural Flavon-3-Ols And Bearing A Lipophilic Decyl Tail Have Been Prepared From Trimethoxy- And Tetramethoxybenzoic Acids Accessed By Lithiation-Carboxylation Reactions. Direct Enolate Acylation Was Preferred Over Baker-Venkataraman Rearrangement When There Were Methoxy Groups At Both The 2- And The 6-Position Of The Benzoic Acid Derivatives.
合成参考文献
参考文献:10.1385/abab:129:1:303
摘要:Hong F, Jönsson LJ, Lundquist K, Wei Y. Oxidation capacity of laccases and peroxidases as reflected in experiments with methoxy-substituted benzyl alcohols. Applied Biochemistry and Biotechnology. 2006 Mar;129(1-3):303–19. doi: 10.1385/abab:129:1:303.
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