![(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylicum acidum Methyl ester hydrochloridum CAS: 565456-77-1 Featured Image](http://cdn.globalso.com/xdbiochems/白色粉末1127.jpg)
![(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylicum acidum Methyl niensis hydrochloride CAS: 565456-77-1](http://cdn.globalso.com/xdbiochems/粉末140.jpg)
(1R,2S,5S)—6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylicum acidum Methyl niensis hydrochloride CAS: 565456-77-1
| Catalogue Number | XD93398 |
| Product Name | (1R,2S,5S)-6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylicum Methyl niensis hydrochloride |
| CAS | 56545-77-1 |
| Formulae hypotheticaela | C9H16ClNO2 |
| M. Pondus | 205.68 |
| Repono Details | Ambiens |
Product Specification
| Aspectus | Pulvis albus |
| Assay | 99% min |
(1R,2S,5S)-6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane-2-carboxylicum hydrochloridum Methyl niensis est mixtum chemicum cum variis applicationibus in investigationis pharmaceuticae et medicamentorum development. clavis usus huius compositionis est sicut clausus chiralis aedificationis in synthesi intermediorum pharmaceuticorum et pharmaceuticae activae (APIs).Unica eius structura bicyclica et chiralitas eam magni pretii faciunt in mixtionibus puris enantiomerice producendis.Compositionem hanc in synthesim inserentes, chemici stereochemisticam regere possunt et proprietates pharmacologicas specificas in moleculis consequentibus creare.Hoc magni ponderis est in progressu medicamento, ubi actio biologica desiderata saepe pendet a dispositione locali moleculi. Praeter (1R,2S,5S)-6,6-DiMethyl-3-aza-bicylo[3.1.0]hexane. Acidum carboxylicum -2-hydrochloridis Methyl niensis praecursor adhibetur ad synthesim quinuclidine-fundatur medicamentorum.Derivationes quinuclidines amplis actionibus biologicis ostenderunt, incluso antipsychotica, anticonvulsante et analgesica proprietates.chemici chemici suas proprietates pharmacokineticas et pharmacodynamicas proprietatibus functionis specificas introducendo possunt mutare potentias therapeuticas. Praeterea haec compositio usum reactant vel catalyst in organicis transformationibus invenit.Ob praesentiam tertiarii aminis et naturas methyl coetus sterically impeditae, varias reactiones chemicas participare potest, sicut amidationi, alkylation et cycloadditioni reactiones.Eius reactivitas et facultas intermedia multiplicia formandi instrumentum versatile in synthesi organica efficit, ut structurae diversorum compositorumque creetur. In summa, (1R,2S,5S)-6,6-DiMethyl-3-aza-bicylo[3.1 .0] Acidum hexane-2-carboxylicum hydrochloridum Methyl niensis pretiosum compositum est in evolutione medicamentorum et organicarum synthesi.Eius chiralitas et unica structura efficiunt compositiones purae enantiomerice et synthesim quinuclidine-fundatae medicamentorum cum specificis proprietatibus pharmacologicis.Eius reactivity etiam utilem reactant et catalyst reddit in variis chemicis transformationibus.Super, haec compositio insignem personam gerit in progressu investigationis pharmaceuticae et in progressu novorum agentium therapeuticorum.
