CAS: 5406-18-8; 3-(4-Methoxyphenyl)Propan-1-Ol

该化合物其结构特征为:丙诺基质,以4-甲基苯基组替代;该化合物一般看起来无色可粉黄黄色液体或固体,视其纯度和温度而定;其水中的中等溶性以及乙醇和乙醇等有机溶剂中的高溶性为人知,这在许多酒精中很常见;甲氧基组的出现,增强了其水恐惧性,同时也有助于其在各种化学反应中的潜在再活动,例如乙化或氧化.3-4-甲基苯基-1-丙醇可能表现出生物活动,使其对制药和化学研究感兴趣.其特性,包括沸点,熔点和特定再活性,可根据样品的条件和纯度而变化.与许多有机化合物一样,适当的处理和安全防范措施对于接触可能危害健康至关重要.

结构式图片

上下游产品

ethanol ethyl (E)-3-(4-methoxyphenyl)prop-2-enoate ethyl 3-(4-methoxyphenyl)propanoate 3-(4-methoxy-phenyl)propionamide 3-(4-hydroxyphenyl)propan-1-ol 3-(4-methoxyphenyl)propyl bromide 3-(4'-methoxy phenyl)-propylchloride Estragole

合成工艺路线路线简述

  • 92409-15-9 = 5406-18-8 + 104-46-1 + 90-05-1 + 1515-95-3 + 104-45-0
    反应条件:1.1C:Ru,S:(Ch2Oh)2,4 H,190°C
    标题:Hydrogen-Transfer Reductive Catalytic Fractionation Of Lignocellulose: High Monomeric Yield With Switchable Selectivity
    作者:By Li,Yilin Et Al
    参考文献:Angewandte Chemie 日期:2023 卷标:62(32) 页码:E202307116
1,2,3-三甲氧基苯置于palladium On Activated Charcoal 吡啶,Sodium Hydroxide,Lithium Aluminium Tetrahydride,三氯化铝,Sodium Dithionite,3-(4-甲氧基苯基)丙醛,氢气,Magnesium,Lithium Bromide体系中,用 四氢呋喃,乙醚,溶剂黄146,丙酮 作为反应溶剂,化学反应 88.5H,反应生成 3-(4-甲氧苯基)-1-丙醇
参考文献:Henley-Smith,Peter; Whiting,Donald A.; Wood,Andrew F.,Journal Of The Chemical Society. Perkin Transactions I,1980,P. 614-622
标题:Henley-Smith,Peter; Whiting,Donald A.; Wood,Andrew F.,Journal Of The Chemical Society. Perkin Transactions I,1980,P. 614-622

海关参考信息

专利信息


专利号:WO-0140193-A1
优先权日:1999-12-03
标题:Method for the synthesis of pyrazolines
发明人:BOLDI ARMEN M
权利人:CHEMRX ADVANCED TECHNOLOGIES I; BOLDI ARMEN M
摘要:The present invention provides a method for the synthesis of compounds of Formula (I). Also claimed are novel intermediates and their methods of synthesis.

专利号:US-2002103381-A1
优先权日:2000-11-30
标 题 :Method for the synthesis of pyrazolines
发明人:BOLDI ARMEN M
摘要:The present invention provides a method for the synthesis of compounds of Formula I: n n n Also claimed are novel intermediates and their methods of synthesis.

专利号:US-7342003-B2
优先权日:2001-10-25
标 题 :Synthesis of 2-aralkyloxyadenosines, 2-alkoxyadenosines, and their analogs
发明人:MOORMAN ALLAN R; SCANNELL MICHAEL; BALASUBRAMANIAN THIAGARAJAN; OUTCALT RUSSELL; LEUNG EDWARD
权利人:KING PHARMACEUTICALS RES & DEV
摘要:Provided is a method for the synthesis of an aralkyloxyadenosine or an alkoxyadenosine. The method includes protecting the hydroxyl sugar groups with a protecting group to produce a protected halogenated adenosine. The protected halogenated adenosine is alkoxylated, and the hydroxyl sugar groups of the protected halogenated adenosine are deprotected to provide the aralkyloxyadenosine or alkoxyadenosine.

专利号:WO-2012152438-A1
优先权日:2011-05-11
标题 :Process for the preparation of nitrate acid ester of organic compounds
发明人:BONFANTI ANNALISA; STORONI LAURA; RONSIN GAEL
权利人:NICOX SA; BONFANTI ANNALISA; STORONI LAURA; RONSIN GAEL
摘要:The present invention relates to a one-step process for the synthesis of nitric acid esters or 15 N isotopically labeled nitrate esters of organic compounds starting from the correspondent alcohols. Formula (I).

专利号:US-2004053999-A1
优先权日:1997-09-17
标题 :Novel compounds and methods for synthesis and therapy
发明人:BISCHOFBERGER NORBERT W; DAHL TERRENCE C; HITCHCOCK MICHAEL J M; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; MILLS ROGER G; WILLIAMS MATTHEW A
摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.

专利号:US-6225341-B1
优先权日:1995-02-27
标 题:Compounds and methods for synthesis and therapy
发明人:BISCHOFBERGER NORBERT W; KIM CHOUNG U; LEW WILLARD; LIU HONGTAO; WILLIAMS MATTHEW A
权利人:GILEAD SCIENCES INC
摘要:Novel compounds are described. The compounds generally comprise an acidic group, a basic group, a substituted amino or N-acyl and a group having an optionally hydroxylated alkane moiety. Pharmaceutical compositions comprising the inhibitors of the invention are also described. Methods of inhibiting neuraminidase in samples suspected of containing neuraminidase are also described. Antigenic materials, polymers, antibodies, conjugates of the compounds of the invention with labels, and assay methods for detecting neuraminidase activity are also described.
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合成参考文献


摘要:Hari, Y.; Aoyama, T.; Shioiri, T., Science of Synthesis Knowledge Updates, (2010) 4, 30.
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