CAS: 3066-90-8; 2,3-Dimethoxy-5-Methylbenzene-1,4-Diol

该化合物是一种有机化合物,其特点是芳香结构,以两种甲氧基组和一个甲基组以及两个羟基组取代苯环,该化合物是一种衍生物,它具有潜在的抗氧化特性,在室温中通常看上去是固体,由于存在甲基氧基组而溶于有机溶剂中,这增加了其水分恐惧性.氢氧基组可以参与氢的结合,影响其再活性和溶解性.2,2-二甲基氧基-5-甲基-1,4-苯乙醇可能展示生物活动,使其在各个领域,包括制药和材料科学中引起兴趣.其合成过程往往涉及对丙酸盐衍生物的甲基化,并且可以使用诸如NMR和质量光谱测量等技术来分析其结构和纯度.与许多有机化合物一样,在实验室环境中处理时应采取安全措施.

结构式图片

欧盟法规

ECHA物质C&L通报

上下游产品

2,3-Dimethoxy-5-methyl-1,4-benzoquinone 2,3-dimethoxy-4-hydroxy-4-(1-propenyl)-2-cyclobuten-1-one ascorbic acid Ubisemihydroquinone ubiquinone-45 ubidecarenone 2-geranyl-5,6-dimethoxy-3-methyl-[1,4]benzoquinone R,11R)-trans-phytyl)-[1,4]benzoquinone2,3-dimethoxy-5-methyl-6-((7R,11R)-trans-phytyl)-[1,4]benzoquinone

合成工艺路线路线简述

  • 合成目标产物 2,3-Dimethoxy-5-Methyl-1,4-Hydroquinone 主要起始原料 2,3-Dimethoxyphenol
  • (文献来源)合成步骤主要原料 2,3-Dimethoxyphenol
📜3,4,5-三甲氧基甲苯置于sodium Tetrahydroborate,双氧水,溶剂黄146体系中,用 甲醇,乙醚,水 用作溶剂,化学反应 192.25H,反应生成2,3-二甲氧基-5-甲基-1,4-苯二酚
参考文献:Reductive Lactonization Of Strategically Methylated Quinone Propionic Acid Esters And Amides
标题:Reductive Lactonization Of Strategically Methylated Quinone Propionic Acid Esters And Amides
摘要:
Doi:10.1021/jo00275A012

海关参考信息

专利信息


专利号:US-6686485-B2
优先权日:2001-04-19
标题:Synthesis of coenzyme Q10, ubiquinone
发明人:WEST DANIEL DAVID
摘要:Processes for the stereospecific synthesis of coenzyme Q10, ubiquinone, are disclosed; a semi synthetic procedure using solanesol derived from tobacco waste as the starting material. The process of the invention results in high yields of isometrically useful compositions containing the optically pure isomers.

专利号:US-3998858-A
优先权日:1975-12-12
标 题:Process for synthesis of coenzymes q
发明人:KIJIMA SHIZUMASA; YAMATU ISAO; HAMAMURA KIMIO; MINAMI NORIO; YAMAGISHI YOUJI; INAI YUICHI
权利人:EISAI CO LTD
摘要:2,3-DIMETHOXY-5-METHYL-6-SUBSTITUTED-1,4-BENZOQUINONE HAVING THE FORMULA: ##STR1## in which R is ##STR2## in which S is an integer of 0 to 11 and A and B stand for hydrogen or may form a direct bond, is prepared by reacting a boric acid ester of 2,3-dimethoxy-5-methyl-1,4-benzohydroquinone with prenol or isoprenol having the above group R and subsequently reacting the resulting borate with a mild oxidant. The compound is useful as coenzyme Q and has various clinical effects.

专利号:US-4057568-A
优先权日:1974-11-22
标 题:Process for synthesis of boric acid ester
发明人:KIJIMA SHIZUMASA; YAMATU ISAO; HAMAMURA KIMIO; MINAMI NORIO; YAMAGISHI YOUJI; INAI YUICHI
权利人:EISAI CO LTD
摘要:2,3-DIMETHOXY-5-METHYL-6-SUBSTITUTED-1,4-BENZOQUINONE HAVING THE FORMULA: ##STR1## in which S is an integer of 0 to 11 and A and B stand for hydrogen or may form a direct bond, n Is prepared by reacting boric acid ester of 2,3-dimethoxy-5-methyl-1,4-benzohydroquinone with prenol or isoprenol having the above group R and subsequently reacting the resulting borate with a mild oxidant. The compound is useful as coenzyme Q and has various clinical effects.

专利号:US-2002156302-A1
优先权日:2001-04-19
标 题:Synthesis of coenzyme Q10, ubiquinone

专利号:US-3939202-A
优先权日:1973-01-31
标题:Process for preparing polyene compounds
发明人:MATSUI MASANAO; KITAMURA SEIICHI; MORIOKA MASAHIRO
权利人:TEIKOKU CHEM IND CO LTD
摘要:Polyene compounds of the formula: ##EQU1## wherein R' is protected or unprotected hydroxyl or a group of the formula: ##EQU2## (in which R' and R'' are each carboxyl or a group convertible into carboxyl on hydrolysis), m is a positive integer and n is 0 or a positive integer, which are useful as intermediates in the synthesis of coenzyme Q, can be produced advantageously through a step for the dehydration of a compound of the formula: ##EQU3## wherein R', m and n are each as defined above.

专利号:US-2004151711-A1
优先权日:2001-04-19
标题 :Synthesis of coenzyme Q10, ubiquinone

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

✅ COA系统入驻 | 共享模式

合成参考文献


参考文献:10.1007/s001140050014
摘要:Deml R, Huth A. Benzoquinones and hydroquinones in defensive secretions of tropical millipedes. Naturwissenschaften. 2000 Feb;87(2):80–2. doi: 10.1007/s001140050014.
参考文献:10.1002/hlca.200800280
摘要:Bouvet M, Malezieux B, Herson P, Villain F. A Ubiquinol‐Based Charge‐Transfer Complex Obtained from a Solvent‐Free Approach. Helvetica Chimica Acta. 2009 Mar;92(3):453–61. doi: 10.1002/hlca.200800280.
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