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(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ&

(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ& Basic information
Product Name:(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ&
Synonyms:Palonosetron Impurity TM1-SR;(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ&;(S-(R*,S*))-(+)-N-(1-phenylethyl)-1- aza bicyclo(;(+)-N-(1(S)-Phenylethyl)-1-azabicyclo[2.2.2]octan-3(R)-amine dihydrochloride, 98%;(+)-N-(1(S)-Phenylethyl)-1-azabicyclo[2.2.2]octan-3(R)-aMine hydrochloride
CAS:120570-09-4
MF:C15H24Cl2N2
MW:303.27046
EINECS:
Product Categories:Chiral Building Blocks;Heterocyclic Building Blocks;Others
Mol File:120570-09-4.mol
(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ& Structure
(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ& Chemical Properties
Melting point 285 °C (dec.)(lit.)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
MSDS Information
(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ& Usage And Synthesis
Uses(3R)-N-[(1S)-1-Phenylethyl]-1-azabicyclo[2.2.2]octan-3-amine Dihydrochloride is the derivative of 3-Quinuclidinone Hydrochloride (Q795795), which is used in the synthesis of cevimeline, a thiolating agent. Also used in the preparation of novel CB1 and CB2 cannabinoid receptor ligands.
(S-(R* S*))-(+)-N-(1-PHENYLETHYL)-1- AZ& Preparation Products And Raw materials
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