CAS: 6280-80-4; 2-(2-Formylphenoxy)Acetic Acid

上下游产品

CAS号90-02-8 水杨醛 | CAS号79-11-8 氯乙酸 | CAS号89-95-2 邻甲基苄醇 | CAS号40359-34-0 (2-甲酰基苯氧基)乙酸甲酯 | CAS号41873-61-4 2-(2-甲酰基苯氧基)乙酸乙酯 | CAS号96-32-2 溴乙酸甲酯 | CAS号271-89-6 苯并呋喃 | CAS号496-41-3 苯并[b]呋喃-2-羧酸 | CAS号40359-34-0 (2-甲酰基苯氧基)乙酸甲酯 | CAS号41873-61-4 2-(2-甲酰基苯氧基)乙酸乙酯 | CAS号654636-49-4 ethyl 2-[2-{bis... | CAS号24590-06-5 2-(2-FORMYL-PHE... | CAS号267644-49-5 2-氨基羰基-5-硝基苯并呋喃 | CAS号124-38-9 二氧化碳 | CAS号56424-77-2 2-(乙氧基羰基甲氧基)苯甲酸乙酯

📜水杨醛置于potassium Carbonate,三氟乙酸体系中,用 水,丙酮 作为反应溶剂,化学反应 20.0H,反应生成 2-甲酰苯氧乙酸
参考文献:Residue-Specific N-Terminal Glycine To Aldehyde Transformation Renders Analytically Pure Single-Site Labeled Proteins
标题:Residue-Specific N-Terminal Glycine To Aldehyde Transformation Renders Analytically Pure Single-Site Labeled Proteins
摘要:在这里,我们展示了 N-甘氨酸向 N-甘氨酸-乙酰胺的残基特异性转化.醛的引入为 N-甘氨酸蛋白质组提供了残基特异性合成的灵活性.
DOI:10.1039/d2Cc04196K

专利信息

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-5977112-A
优先权日:1995-04-20
标 题:Process of making substituted benzofurans
发明人：BATHE ANDREAS; HELFERT BERND; BOTTCHER HENNING; SCHUSTER KURT
权利人:MERCK PATENT GMBH
摘要:Benzofurans of the formula I ##STR1## and their salts in which R 1 , R 2 and X have the meanings indicated in claim 1, are suitable as intermediates in the synthesis of medicaments and show effects on the central nervous system.

专利号:US-8926801-B2
优先权日:2009-01-16
标题 :Methods of electrospray chemical synthesis and device for use therein
发明人：REHMAN ATIQ
权利人:REHMAN ATIQ; CANAM BIORES INC
摘要:The present invention relates to methods of production of chemical bonds and subsequent molecules by electrospray ionization and the design of an electrospray chemical synthesizer, for use in chemical synthesis and expedited organic chemical reactions.

专利号:US-6531470-B1
优先权日:1998-01-23
标题:Oxazolidinone combinatorial libraries, compositions and methods of preparation
发明人：GORDEEV MIKHAIL F; LUEHR GARY W; PATEL DINESH V; NI ZHI-JIE; GORDON ERIC
权利人:UPJOHN CO
摘要:Oxazolidinones and methods for their synthesis are provided. Also provided are combinatorial libraries comprising oxazolidinones, and methods to prepare the libraries. Further provided are methods of making biologically active oxazolidinones as well as pharmaceutically acceptable compositions comprising the oxazolidinones. The methods of library preparation include the attachment of oxazolidinones to a solid support. The methods of compound preparation in one embodiment involve the reaction of an iminophosphorane with a carbonyl containing polymeric support.