Cas 147225-38-5,2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime

147225-38-5

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Basic information

Product Name: 2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime
Synonyms: 2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime
CAS NO:147225-38-5
Molecular Formula:
Molecular Weight: 366.46
EINECS: N/A
Product Categories: N/A
Mol File: 147225-38-5.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: 2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime(CAS DataBase Reference)
NIST Chemistry Reference: 2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime(147225-38-5)
EPA Substance Registry System: 2,4-bis(2-methoxyphenyl)-3-azabicyclo[3.3.1]nonan-9-one oxime(147225-38-5)

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: 147225-38-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 147225-38-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,7,2,2 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 147225-38:
(8*1)+(7*4)+(6*7)+(5*2)+(4*2)+(3*5)+(2*3)+(1*8)=125
125 % 10 = 5
So 147225-38-5 is a valid CAS Registry Number.

147225-38-5Upstream product

34143-13-0 2,4-bis(2-methoxyphenyl)-3-azabicyclo<3.3.1>nonan-9-one

147225-38-5Downstream Products

147225-38-5Relevant articles and documents

Synthesis, complete NMR spectral assignments, and antifungal screening of new 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-one oxime derivatives

Parthiban, Paramasivam,Rathika, Paramasivam,Park, Keun Soo,Jeong, Yeon Tae

experimental part, p. 79 - 93 (2010/07/10)

A series of differently substituted 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9- one oximes have been synthesized and their 1H and 13C NMR chemical shifts have been unambiguously assigned using H,H-COSY, NOESY, HSQC, and HMBC spectral data

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