Cas 135424-79-2,8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane

135424-79-2

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Basic information

Product Name: 8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane
Synonyms: 8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane
CAS NO:135424-79-2
Molecular Formula:
Molecular Weight: 439.554
EINECS: N/A
Product Categories: N/A
Mol File: 135424-79-2.mol
Article Data: 1

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: 8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane(CAS DataBase Reference)
NIST Chemistry Reference: 8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane(135424-79-2)
EPA Substance Registry System: 8-β-(xanthen-9'''-carbonyloxy)-N-phenethyl-3-azabicyclo<3.2.1>octane(135424-79-2)

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: 135424-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 135424-79-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,4,2 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 135424-79:
(8*1)+(7*3)+(6*5)+(5*4)+(4*2)+(3*4)+(2*7)+(1*9)=122
122 % 10 = 2
So 135424-79-2 is a valid CAS Registry Number.

135424-79-2Upstream product

135424-79-2Downstream Products

135424-79-2Relevant articles and documents

Synthesis and structural, conformational, and pharmacological study of some esters derived from 3-phenethyl-3-azabicyclo[3.2.1]octan-8-β-ol and the corresponding N-endo-methyl quaternary derivatives

Izquierdo,Arias,Galvez,Rico,Ardid,Sanz,Fonseca,Orjales,Innerarity

, p. 554 - 558 (2007/10/02)

A series of 8-β-acyloxy-3-phenethyl-3-azabicyclo[3.2.1]octane and its N-endo methiodides were synthesized and studied by 1H and 13C NMR spectroscopy, and the crystal structure of 8-β-p-chlorobenzoyloxy-3-phenethyl-3-azabicyclo[3.2.1]

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