Cas 1395407-86-9,2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one

1395407-86-9

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Basic information

Product Name: 2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one
Synonyms: 2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one
CAS NO:1395407-86-9
Molecular Formula:
Molecular Weight: 312.196
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: 2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one(1395407-86-9)
EPA Substance Registry System: 2-(3,4-dichlorophenyl)-1-[(1R,5S)-2-oxa-6-azabicyclo[3.3.1]non-3-en-6-yl]ethan-1-one(1395407-86-9)

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: 1395407-86-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1395407-86-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,4,0 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1395407-86:
(9*1)+(8*3)+(7*9)+(6*5)+(5*4)+(4*0)+(3*7)+(2*8)+(1*6)=189
189 % 10 = 9
So 1395407-86-9 is a valid CAS Registry Number.

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1395407-86-9Relevant academic research and scientific papers

From mannose to morphan analogues: Methyl α-d-mannoside as chiral building block for the synthesis of mono- and bicyclic σ receptor ligands

Wiedemeyer, Kathrin,Wuensch, Bernhard

, p. 24 - 29 (2013/01/14)

Previously the synthesis and high σ1 receptor affinity of mannose derived pyrans 3-5 with equatorially oriented amino groups have been reported. Herein the synthesis and receptor affinities of the corresponding axially substituted pyrans and ox

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