Cas 122846-70-2,3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide

122846-70-2

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Basic information

Product Name: 3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide
Synonyms: 3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide
CAS NO:122846-70-2
Molecular Formula:
Molecular Weight: 502.393
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide(CAS DataBase Reference)
NIST Chemistry Reference: 3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide(122846-70-2)
EPA Substance Registry System: 3-(1-methyl-1-azabicyclo<2.2.2>octyl) 2-hydroxy-3-(4-morpholinyl)-2-phenylpropionate iodide(122846-70-2)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 122846-70-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122846-70-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,4 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 122846-70:
(8*1)+(7*2)+(6*2)+(5*8)+(4*4)+(3*6)+(2*7)+(1*0)=122
122 % 10 = 2
So 122846-70-2 is a valid CAS Registry Number.

122846-70-2Upstream product

122846-70-2Downstream Products

122846-70-2Relevant academic research and scientific papers

Synthesis of some 3-(1-azabicyclo[2.2.2]octyl) 3-amino-2-hydroxy-2-phenylpropionates: Profile of antimuscarinic efficacy and selectivity

Audia,McPherson,Weitzberg,Rzeszotarski,Sturm,Kachur,Abreu,Kaiser

, p. 307 - 310 (2007/10/02)

A series of 3-quinuclidinyl atrolactate [3-(1-azabicyclo[2.2.2]octyl) 2-hydroxy-2-phenylpropionate, QNA] derivatives in which the methyl group of the parent is substituted with a tertiary amino substituent was prepared and tested for antimuscarinic activi

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