CAS: 59276-28-7; 1-(Dimethoxymethyl)-3-Methoxybenzene

该化合物是一种有机化合物,其特点是芳香结构,包括一个苯环,由甲基和甲氧基组替代,这些替代成分的存在影响其化学特性,如溶性,再活性等.典型的情况是,与甲基氧组的化合物具有中等极化性,这可以提高其在极地溶剂中的溶解性,同时保持苯环的某些疏水特性.该化合物可参与电子嗜血替代反应,一种芳香化合物的常见行为,还可因存在甲氧基组而经历各种典型的醚和酒精变异.其应用可能跨越诸如有机合成,制药和材料科学等领域,可以作为较复杂的分子的中间或建筑块.在处理和储存时,应参考安全数据,如同任何化学物质一样,以确保采取适当的预防措施.

结构式图片

相似化合物

2186-92-7 5368-81-0 108593-44-8

MSDS等安全信息

    上下游产品

    3-(1,3-dioxolan-2-yl)-phenylbromide sodium methylate 3-methoxy-benzaldehyde trimethyl orthoformate Acetic acid (E)-4-(2-dimethoxymethyl-6-methoxy-phenyl)-1-ethyl-but-2-enyl ester meso-1,2-bis-(3'-methoxyphenyl)-1,2-dimethoxyethane d,l-1,2-bis-(3'-methoxyphenyl)-1,2-dimethoxyethane m-methoxybenzyl chloride

    合成工艺路线路线简述

      间甲氧基苯甲醇置于in(Oso2Cf3)3 Manganese(Iv) Oxide体系中,用 二氯甲烷 作为反应溶剂,化学反应 24.0H,反应生成 1-(二甲氧基甲基)-3-甲氧基苯
      参考文献:Sequential And Tandem Oxidation/acetalization Procedures For The Direct Generation Of Acetals From Alcohols
      标题:Sequential And Tandem Oxidation/acetalization Procedures For The Direct Generation Of Acetals From Alcohols
      摘要:Alcohols Are Transformed Directly Into Either Acyclic Or Cyclic Acetals In Both Tandem And Sequential Oxidation/acetalization Processes Using Manganese Dioxide,Trialkyl Orthoformates And Catalytic Quantities Of Indium Triflate. (C) 2007 Elsevier Ltd. All Rights Reserved.
      DOI:10.1016/j.Tetlet.2007.05.060

      海关参考信息

      专利信息


      专利号:US-5763681-A
      优先权日:1989-09-06
      标 题 :Synthesis of stable, water-soluble chemiluminescent 1,2-dioxetanes and intermediates therefor
      发明人:EDWARDS BROOKS; JUO RHOU-RONG
      权利人:TROPIX INC
      摘要:A novel synthesis of compound having the formula: ##STR1## wherein T is a stabilizing spiro-linked polycycloalkylidene group, R 3 is a C 1 -C 20 alkyl, aralkyl or heteroatom containing group, Y is an aromatic fluorescent chromophore, and Z is a cleavable group which, when cleaved, induces decomposition of the dioxetane ring and emission of optically detectable light, is disclosed. A tertiary phosphorous acid alkyl ester of the formula: n n (R.sup.1 O).sub.3 P n n wherein R 1 is a lower alkyl group, is reacted with an aryl dialkyl acetal produced by reacting a corresponding aryl aldehyde with an alcohol of the formula: n n R.sup.3 OH n n wherein R 3 is as defined above, to produce a 1-alkoxy-1-aryl-methane phosphonate ester of the formula: ##STR2## reacting the phosphonate with base to produce a phosphonate-stabilized carbanion, reacting the carbanion with a ketone of the formula: ##STR3## wherein T is as defined above, to produce an enol ether of the formula: ##STR4## then oxygenating the double bond in the enol ether to give the corresponding 1,2-dioxetane compound.

      专利号:US-5936132-A
      优先权日:1994-03-11
      标题 :Alkene intermediates and synthesis thereof
      发明人:MATSUMOTO MASAKATSU
      摘要:A chemiluminescent 1,2-dioxetane derivative having a formula (I): ##STR1## wherein R 1 and R 4 each represent, individually, hydrogen, an alkyl group, an alkoxyl group, a hydroxyl group, or --OS;(R 9 R 10 R 11 ) in which R 9 , R 10 and R 11 each represent an alkyl group; R 2 , R 3 , R 5 and R 6 each represent, individually, hydrogen or an alkyl group, provided that R 2 , R 3 , R 5 and R 6 each cannot be hydrogen at the same time, and that R 2 and R 3 , and R 5 and R 6 , each taken together, can form a cycloalkyl group; R 7 represents an alkyl group; R 8 represents hydrogen, an alkoxyl group, a phosphate salt group, or --OSi(R 9 R 10 R 11 ); intermediates for synthesizing the above 1,2-dioxetane derivative; and methods of producing the intermediates are provided.

      专利号:US-2023381213-A1
      优先权日:2022-05-31
      标题 :Synthesis and uses of ginsenoside compound k derivatives
      发明人:CHE CHI-MING; LIU YUNGEN; HE JILIN; LOK CHUN-NAM
      权利人:UNIV HONG KONG; LABORATORY FOR SYNTHETIC CHEMISTRY AND CHEMICAL BIOLOGY LTD
      摘要:A nontoxic anticancer compound is a derivative of 20-O-β-(D-glucopyranosyl)-20(S)-protopanaxadiol (CK) having at least one of the glucose hydroxyl groups replaced with at least one acetal group. The derivative enhances binding to a mitochondrial membrane protein and is more cytotoxic to cancerous cells than CK. The derivative can be an acetal of an unsubstituted or substituted aromatic group, such as an acetal formed from a substituted 1-(dimethoxymethyl)-benzene. One or more of the CK derivative (CKD) anticancer compounds can be used as an active portion of an anticancer medicament.

      专利号:WO-9103479-A1
      优先权日:1989-09-06
      标题:Synthesis of stable, water-soluble chemiluminescent 1,2-dioxetanes and intermediates therefor

      专利号:US-5225584-A
      优先权日:1989-09-06
      标 题 :Synthesis of stable water-soluble chemiluminescent 1,2-dioxetanes and intermediates therefor

      专利号:EP-0441948-A4
      优先权日:1989-09-06
      标 题:Synthesis of stable, water-soluble chemiluminescent 1,2-dioxetanes and intermediates therefor
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      合成参考文献


      参考文献:10.1007/bf00430879
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