CAS: 32723-67-4; 4-Methoxy-3-Methylbenzaldehyde

该化合物是苯环上以甲氧基和甲基替代物为特征的芳香藻.该化合物的特征是:甲氧组(-OCH)在准位置,甲基组( -CH)在甲氨酰功能组( CHO)的元位置.该产品一般是一种无色的黄色液体,具有甜美的香味,与青色的香水相仿,与芳香的香气有共鸣,与肛火形成共鸣;该化合物在乙醇和乙醚等有机溶剂中溶解,但在水中溶性有限.该混合物在各种应用中使用,包括调味剂,香味成分和有机合成中的中间.此外,4-甲基三甲基苯甲酰胺可以对甲胺作典型的反应,如氧化和凝聚,使其在合成更复杂的有机分子中成为适应性建筑块.在处理该化合物时,应当采取安全防范措施,因为它可能会对皮肤和眼睛造成刺激.

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CAS号4685-47-6 3,4-二甲基苯甲醚 | CAS号578-58-5 邻甲基苯甲醚 | CAS号68-12-2 N,N-二甲基甲酰胺 | CAS号108-24-7 乙酸酐 | CAS号6738-23-4 2,4-二甲基苯甲醚 | CAS号74-90-8 氢氰酸 | CAS号14804-31-0 4-溴-2-甲基苯甲醚 | CAS号114787-91-6 4-甲氧基-3-甲基苄醇 | CAS号108125-07-1 3-甲基-4-甲氧基苄胺 | CAS号60736-71-2 4-甲氧基-3-甲基氯苄 | CAS号4513-73-9 4-甲氧基-3-甲基苯乙酸 | CAS号22442-47-3 3-(4-甲氧基-3-甲基-苯基)-丙酸 | CAS号6738-23-4 2,4-二甲基苯甲醚 | CAS号75391-57-0 4-甲氧基-3-甲基苯乙腈 | CAS号114787-91-6 4-甲氧基-3-甲基苄醇 | CAS号6880-04-2 4-甲氧基-3-甲基苯甲酸 | CAS号105-67-9 2,4-二甲基苯酚 | CAS号18149-08-1 2-(3-氯-4-甲氧基-苯基)-乙酰胺

合成工艺路线路线简述

    2,4-二甲基-1-甲氧基苯置于核黄素,2',3',4',5'-四乙酸酯体系中,用 水,叔丁醇 作为反应溶剂,25.0 °C,101.33 Kpa 条件下,反应生成 4-甲氧基-3-甲基苯甲醛
    参考文献:黄素光催化甲苯和邻苯二胺有氧交叉脱氢偶联苯并咪唑的简便合成
    标题:黄素光催化甲苯和邻苯二胺有氧交叉脱氢偶联苯并咪唑的简便合成
    摘要:在此,我们展示了通过甲苯和邻苯二胺的黄素光催化有氧氧化交叉脱氢偶联来实现苯并咪唑的绿色原子经济合成.所提出的无金属反应在可见光照射下在甲醇/H2O 中进行,仅消耗大气中的分子氧并仅产生水作为废物.
    DOI:10.1039/d3Ob00113J

    海关参考信息

    专利信息


    专利号:US-6121054-A
    优先权日:1997-11-19
    标 题 :Method for separation of liquid and solid phases for solid phase organic syntheses
    发明人:LEBL MICHAL
    权利人:TREGA BIOSCIENCES INC
    摘要:A simple, efficient apparatus and method for separation of solid and liquid phases useful in methods of high-throughput combinatorial organic synthesis of large libraries or megaarrays of organic compounds is disclosed. The apparatus and method are useful, whether as part of an automated, robotic or manual system for combinatorial organic synthesis. In a preferred embodiment, an apparatus and method of removal of liquid phase from solid phase compatible with microtiter plate type array(s) of reaction vessels is disclosed.

    专利号:US-5175302-A
    优先权日:1987-07-13
    标 题 :Nucleophilic fluoroalkylation of aldehydes
    发明人:STAHLY G PATRICK
    权利人:ETHYL CORP
    摘要:Aryl difluoromethyl sulfone adds to aldehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.

    专利号:US-4837327-A
    优先权日:1987-07-13
    标 题 :Process for nucleophilic fluoroalkylation of aldehydes
    发明人:STAHLY G PATRICK
    权利人:ETHYL CORP
    摘要:Aryl difluoromethyl sulfone adds to alkehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.

    专利号:US-4999429-A
    优先权日:1989-01-09
    标 题 :Process for the preparation of α,α,β-1-trifluoro-1-olefinic derivatives
    发明人:STAHLY G PATRICK
    权利人:ETHYL CORP
    摘要:Aryl difluoromethyl sulfone adds to aldehydes under phase transfer conditions to give novel substituted alcohols of the general formula n n RCH(OH)CF.sub.2 SO.sub.2 Ar (I) n n wherein R is an aryl, cycloaliphatic, sec- or tert-aliphatic, or heterocyclic group and Ar is an aryl group. The substituted alcohols of formula I are of particular utility as intermediates in the synthesis of a variety of useful end products. For example, the products of formula I may be utilized in desulfonylation reactions, oxidation reactions and fluorination reactions.

    专利号:US-6045755-A
    优先权日:1997-03-10
    标题 :Apparatus and method for combinatorial chemistry synthesis
    发明人:LEBL MICHAEL; POKORNY VIT; KRCHNAK VIKTOR
    权利人:TREGA BIOSCIENCES INC
    摘要:In a first embodiment, this invention includes an integrated robot apparatus for performing combinatorial chemistry synthesis protocols and having interchangeable work-stations, robot arm tools, and reaction vessels and reaction vessel arrays. The work-stations and tools are specialized to perform tasks necessary for the synthesis in a plurality of the reaction vessels grouped in a plurality of the reaction vessel arrays. Preferably, these elements function interchangeably because they have standardized sizes and conformation. The work-stations and tools include those for fluid dispensing or aspirating from individual reaction vessels or from all the reaction vessels in an array simultaneously. The reaction vessels can include, alternatively, stackable, ball-sealed reaction vessels, microtitre-like reaction vessel arrays, arrays of independent reaction vessels, valve-sealed reaction vessels, septum-sealed reaction vessels, and syringe reaction vessels. In alternative embodiments, this invention includes these work-stations, tools, reaction vessels and reaction vessel arrays in various combinations or sub-combinations either for use in partially integrated robots or for manual or standalone use.

    专利号:US-5916899-A
    优先权日:1996-10-18
    标 题:Isoquinoline derivatives and isoquinoline combinatorial libraries
    发明人:KIELY JOHN S; GRIFFITH MICHAEL C
    权利人:TREGA BIOSCIENCES INC
    摘要:The present invention provides the synthesis of heterocyclic compounds based on the isoquinoline ring. More specifically, the invention provides novel isoquinolines as well as novel libraries comprised of many such compounds, and methods of synthesizing the libraries.
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    主要参考文献

    [参考文献]: Tamer Awad, Et Al. Gc-Ms Analysis Of Acylated Derivatives Of The Side-Chain Regioisomers Of 4-Methoxy-3-Methyl-Phenethylamines Related To Methylenedioxymethamphetamine. J Chromatogr Sci. 2007 Sep;45(8):477-85.

    合成参考文献


    摘要:S109 | PARCEDC | List of 7074 potential endocrine disrupting compounds (EDCs) by PARC T4.2 | DOI:10.5281/zenodo.10944198
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