CAS: 645-36-3; 2,2-Diethoxyethanamine

上下游产品

CAS号5344-23-0 2,2-二乙氧基乙醛 | CAS号6136-93-2 二乙氧基乙腈 | CAS号621-62-5 氯乙醛缩二乙醇 | CAS号2032-35-1 2-溴-1,1-二乙氧基乙烷 | CAS号51806-20-3 1,1-Diethoxy-2-... | CAS号105-57-7 1,1-二乙氧基乙烷 | CAS号34560-16-2 1,1-二乙氧基-2-硝基乙烷 | CAS号108230-73-5 3-N-(2',2'-diet... | CAS号61189-99-9 2,2-二乙氧基乙酰胺 | CAS号6065-82-3 二乙氧基乙酸乙酯 | CAS号34167-66-3 5,6,7,8-四氢-咪唑[1... | CAS号34784-07-1 8-氯异喹啉 | CAS号42398-73-2 6-甲基异喹啉 | CAS号345311-03-7 7-B°C-5,6,7,8-四... | CAS号34784-04-8 5-溴异喹啉 | CAS号5768-55-8 6,7,8,9-四氢-5H-咪... | CAS号176492-83-4 N-(4-亚乙基二氧环己烷)-... | CAS号39989-39-4 7-甲氧基异喹啉 | CAS号1721-93-3 1-甲基异喹啉 | CAS号1810-57-7 Phenol,5-[[(2,2...

2,2-二乙氧基乙酰胺置于lithium Aluminium Tetrahydride体系中,用 四氢呋喃 作为反应溶剂,化学反应生成 氨基乙醛缩二乙醇
参考文献:Bouvier,P. Et Al.,European Journal Of Medicinal Chemistry,1976,Vol. 11,P. 271-278
标题:Bouvier,P. Et Al.,European Journal Of Medicinal Chemistry,1976,Vol. 11,P. 271-278

专利信息

专利号:US-9079824-B2
优先权日:2010-07-06
标 题:Method for the synthesis of an amino acetal
发明人：LOH TECK PENG; TIAN JIESHENG
权利人:LOH TECK PENG; TIAN JIESHENG; UNIV NANYANG TECH
摘要:The present invention relates to a method for the synthesis of an α amino acetal, comprising (i) oxidizing a tertiary amine in the presence of a copper catalyst, at least one oxidant and a solvent, or (ii) reacting a secondary amine and an aliphatic aldehyde in the presence of a copper catalyst, at least one oxidant and a solvent.

专利号:US-2004147775-A1
优先权日:2002-12-23
标 题:Process for the synthesis of 3.3A.6.6A-tetrahydro-2H-cyclopentan[b]furan-2-one
发明人：HENEGAR KEVIN EDWARD; CEBULA MATEUSZ
摘要:The present invention relates to a process for the synthesis of 3,3a,6,6a-tetrahydo-2H-cyclopentan[b]furan-2-one.

专利号:US-9206222-B2
优先权日:2009-06-29
标题:Solid phase peptide synthesis of peptide alcohols
发明人：CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN
权利人:CAUSSIL-AMBLARD MURIEL; MARTINEZ JEAN; TAILHADES JULIEN; CENTRE NAT RECH SCIENT
摘要:The present invention relates to the synthesis of depsipeptides on solid phase support. Said depsipeptides are then implicated in a solution phase O—N acyl shift enabling to obtain the corresponding peptide alcohols.

专利号:US-7109377-B2
优先权日:1996-10-16
标 题:Synthesis of combinatorial libraries of compounds reminiscent of natural products
发明人：SCHREIBER STUART L; SHAIR MATTHEW D; TAN DEREK S; FOLEY MICHAEL A; STOCKWELL BRENT R
权利人:HARVARD COLLEGE
摘要:The present invention provides complex compounds reminiscent of natural products and libraries thereof, as well as methods for their production. The inventive compounds and libraries of compounds are reminiscent of natural products in that they contain one or more stereocenters, and a high density and diversity of functionality. In general, the inventive libraries are synthesized from diversifiable scaffold structures, which are synthesized from readily available or easily synthesizable template structures. In certain embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from a shikimic acid based epoxyol template. In other embodiments, the inventive compounds and libraries are generated from diversifiable scaffolds synthesized from the pyridine-based template isonicotinamide. The present invention also provides a novel ortho-nitrobenzyl photolinker and a method for its synthesis. Furthermore, the present invention provides methods and kits for determining one or more biological activities of members of the inventive libraries. Additionally, the present invention provides pharmaceutical compositions containing one or more library members.

专利号:US-9546161-B2
优先权日:2001-07-16
标题:Synthesis of UDP-glucose: N-acylsphingosine glucosyl transferase inhibitors
发明人：HIRTH BRADFORD H; SIEGEL CRAIG
权利人:GENZYME CORP
摘要:Disclosed is a novel enantiomeric synthesis ceramide-like inhibitors of UDP-glucose: N-acylsphingosine glucosyltransferase. Also disclosed are novel intermediates formed during the synthesis.

专利号:US-4777257-A
优先权日:1983-08-25
标题:Certain tetrahydronaphthyl or indanylcarboxylates and derivatives thereof which inhibit the synthesis of thromboxane
发明人：KANAO MUNEFUMI
权利人:DAIICHI SEIYAKU CO
摘要:Benzocycloalkane derivatives of the formula (I) ##STR1## wherein: Z represents a methylene group or an ethylene group, either one of R 1 and R 2 represents --(CH 2 ) m --COOR 3 and the other represents ##STR2## wherein R 3 represents a hydrogen atom or an alkyl group having 1 to 6 carbon atoms, n represents an interger of 1 to 6 and m represents an interger of 0 to 5, and the physiologically acceptable salts thereof; having a strong and selective inhibition activity of thromboxane A 2 synthesis.