CAS: 26501-54-2; Tetrabutylammonium Nitrite

上下游产品

tetrabutylammomium bromide tetrabutyl ammonium fluoridetetrabutylammonium nitrate naphthalene-1-carboxylic acid butyl ester nitrogen(II) oxide

📜四丁基溴化铵置于potassium Nitrite体系中,用 水 用作溶剂,化学反应生成四丁基亚硝酸铵
参考文献:部分[n+4444]基离子液体的离子交换合成及热特性
标题:部分[n+4444]基离子液体的离子交换合成及热特性
摘要:摘要 使用四丁基铵阳离子 [n + 4444 ] 和无机阴离子如 Bf 4-,No 3-,No 2-,Scn-,Bro 3-,Io 3-,Pf 6-和 Hco 3-合成了八种盐.离子交换法.使用热重法,差示扫描量热法和红外光谱法对这些离子液体 (Il) 进行了表征.热物理性质,如密度,体积膨胀,熔化热,固-固转变热,比热容和热能储存能力被确定.在某些情况下,在熔点以下观测到的固-固转变的总热量超过了熔化热.在固相和液相中测定样品的热导率.
Doi:10.1016/j.Tca.2013.01.003

专利信息

专利号:US-10851130-B2
优先权日:2018-01-29
标题:Chemical synthesis method of Plesiomonas shigelloides serotype O51 O-antigen oligosaccharide
发明人：YIN JIAN; HU JING; SEEBERGER PETER; QIN CHUNJUN
权利人:UNIV JIANGNAN; MAX PLANCK INST OF COLLOIDS AND INTERFACES
摘要:The present disclosure discloses the chemical synthesis method of the Plesiomonas shigelloides serotype O51 O-antigen oligosaccharide, belonging to the field of chemistry. Source-abundant D-glucose, L-fucose, D-glucosamine and the like are used as raw materials to prepare three glycosylation building blocks, the synthetic route composed of 11 reaction modules is designed, and through the optimization of protecting group and the optimization of the time of introducing functional group, the preparation of the target oligosaccharide chain is successfully achieved. The oligosaccharide chain prepared in the present disclosure has the advantages of cheap and easy-to-get raw materials, and simple and easy-to-repeat preparation method. The present disclosure will have good application prospects in the aspects of development of new drugs and vaccines of Plesiomonas shigelloides , and the like.

专利号:US-8697862-B2
优先权日:2008-05-16
标题 :Synthesis of galactoside inhibitors
发明人：NILSSON ULF
权利人:NILSSON ULF; GALECTO BIOTECH AB
摘要:Novel synthesis routes for preparation of thiodigalactosides and intermediates are presented. The method includes the use of a 3-azido-galactosyl thiouronium salt derivative, which is activated to the corresponding thiol in situ, which in turn is directly reacted with a 3-azido-galactosyl bromide resulting in the 3,3′-di-azido-thio-di-galactoside before the thiol has a chance to reduce the azido 10 group. Hence, in situ formation of the 3-azido-galactosyl thiol from the thiouronium salt is essential in the synthesis procedure, because any other method that generate the thiol separately results in extensive unwanted azide reduction.

专利号:US-2024409571-A1
优先权日:2023-06-08
标 题:Chemoenzymatic synthesis of n-acetylated gangliosides and glycosphingosines
发明人：CHEN XI; YU HAI; MISHRA BIJOYANANDA; ZHENG ZIMIN; AGRAHARI ANAND KUMAR; GUCCHAIT ARIN
权利人:UNIV CALIFORNIA
摘要:Described herein are novel stable 9-N-, 8-N-, and 7-N-acetyl analogues of instable 9-O-acetyl, 8-O-acetyl, and 7-O-acetyl b-series gangliosides and glycosphingosines, including GD3, GD2, GD1b, GT1b, GQ1b, and their glycosphingosines. Chemoenzymatic methods for the production of the stable 9-N-, 8-N-, and 7-N-acetyl analogues are also described herein.

专利号:WO-2009139719-A9
优先权日:2008-05-16
标 题 :Novel synthesis of galactoside inhibitors

专利号:CA-2724064-C
优先权日:2008-05-16
标题 :Synthesis of galactoside inhibitors

专利号:WO-2018002957-A2
优先权日:2016-06-29
标题 :A method for synthesis of 6-deoxy-l-hexoses from l-rhamnose