CAS: 1836-42-6; Benzyltriethylammonium (Hydroxide)

相似化合物

5400-94-2 85874-45-9 5197-95-5

上下游产品

N-benzyl-N,N,N-triethylammonium chloride benzyl chloride triethylamine2-(4-chlorophenyl)-2-hydroxymethylpropionitrile ethyl-α-(1-carboxyethyl)amino-γ-oxo-γ-phenylbutyrate

氯化苄置于silver(L) Oxide体系中,化学反应生成苄基三乙基氢氧化铵
参考文献:Ladenburg; Struve,Chemische Berichte,1877,Vol. 10,P. 46
标题:Ladenburg; Struve,Chemische Berichte,1877,Vol. 10,P. 46

专利信息

专利号:US-2009264648-A1
优先权日:2008-01-14
标题:Synthesis of pyrazoles
发明人：CHEW WARREN; WANG ZHENG; CHEAL GLORIA; BERTRAND MARTIAL; POTOSKI JOHN; MIRMEHRABI MAHMOUD; NENCINI ARIANNA; ZANALETTI RICCARDO
权利人:WYETH CORP; SIENA BIOTECH SPA
摘要:The present invention provides compounds and compositions, methods of making them, and methods of using them to modulate α7 nicotinic acetylcholine receptors and/or to treat any of a variety of disorders, diseases, and conditions. Provided compounds can affect, among other things, neurological, psychiatric and/or inflammatory system.

专利号:US-5510528-A
优先权日:1993-04-08
标题:Preparation of halomethylbenzoly cyanides and novel halomethylbenzoyl cyanides
发明人：ISAK HEINZ; WETTLING THOMAS; KEIL MICHAEL; WOLF BERND; DOETZER REINHARD
权利人:BASF AG
摘要:A process for preparing halomethylbenzoyl cyanides I n n Ph-CO-CN I n n (Ph=phenyl radical substituted by chloromethyl or bromomethyl which, if desired, can additionally carry 1-4 further radicals) by reacting halomethylbenzoyl chlorides II n n Ph-CO-Cl II n n with an alkali metal cyanide or transition metal cyanide, if appropriate in an organic diluent, and novel halomethylbenzoyl cyanides I' ##STR1## (X=halogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkoxy, CF 3 , C 1 -C 5 -alkyl-(C 1 -C 5 -alkyl)hydroxyimino or C 1 -C 5 -alkyl-(C 2 -C 5 -alkenyl)hydroxyimino; m=0 to 4 and Y=chloromethyl or bromomethyl) are described. n The halomethylbenzoyl cyanides I are important intermediates for the synthesis of plant protection agents.

专利号:US-6040440-A
优先权日:1998-03-06
标题:Hypophosphite deoxygenation reactions in the synthesis of erythromycin derivatives
发明人：GRAHAM ALEXANDRA E; THOMAS ALBERT V; YANG RACHEL R P
权利人:ABBOTT LAB
摘要:A process for the preparation of 4''-deoxyerythromycins, having the formula: wherein R is H or OH, R1 is H or loweralkyl, and R2 is H or CH3 by treatment of the starting material, 2'-O-acetyl-4''-imidazolylthiocarbamoyl-erythromycin, with a hypophosphite reagent, in a water-miscible protic solvent optionally comprising a phase transfer agent. In a preferred embodiment, the water-miscible solvent is an alcohol and the starting material is reacted with sodium hypophosphite, ACVA and tetra-n-butylammonium hydroxide.

专利号:WO-2018229729-A1
优先权日:2017-06-15
标 题 :Combined gasification and catalytic decomposition for the production of hydrogen and synthesis gas from hydrocarbons
发明人：ALBAHILY KHALID; VISWANATH VINU K; AL-SABBAN BEDOUR; RAVON UGO; ALZAILAIE ABDULRAHMAN MOOSA
权利人:SABIC GLOBAL TECHNOLOGIES BV
摘要:Processes, systems, and catalysts for the production of a gaseous hydrogen (H2) stream and a synthesis gas stream comprising H2 and carbon monoxide (CO) are described. A process can include contacting a gaseous mixture of hydrocarbons having 1 to 5 carbon atoms (C1-5) with a hydrocarbon decomposition catalyst under non-oxidizing conditions suitable to produce a gaseous H2 stream and a carbon coated hydrocarbon decomposition catalyst, and contacting the carbon coated hydrocarbon decomposition catalyst with water under conditions suitable to produce a synthesis gaseous stream comprising H2 and CO in a H2:CO molar ratio of about 1 : 1 and a regenerated hydrocarbon decomposition catalyst. The hydrocarbon decomposition catalyst can be a hollow zeolite catalyst, a pyrochlore catalyst, an olivine catalyst, a spinel catalyst, or mixtures thereof.

专利号:EP-3567040-B1
优先权日:2013-06-24
标 题 :Method for the preparation of intermediates useful for the synthesis of [1,2,4]-triazolo[4,3-a]pyridines

专利号:US-10011631-B2
优先权日:2015-12-01
标题 :Stapled helical peptides and methods of synthesis
发明人：LI XUECHEN; LEE CHI-LUNG; XU JIAOCHAO
权利人:UNIV HONG KONG
摘要:The present disclosure relates to the design and generation of stapled helical peptides that perturb protein-protein interactions (PPIs). The methods disclosed herein for preparing stapled peptides involve providing a peptide having a first amino acid that is functionalized with a salicylaldehyde ester side group and a second amino acid functionalized with a 1,2-hydroxyl amine side group; reacting the first and second amino acids to generate an N,O-benzylidene acetal moiety; and performing acidolysis of the resultant N,O-benzylidene acetal moiety to generate the stapled peptide. In many forms, the stapled helical peptides described herein are not hydrophobic.