Cas 1174000-61-3,4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide

1174000-61-3

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Basic information

Product Name: 4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide
Synonyms: 4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide
CAS NO:1174000-61-3
Molecular Formula:
Molecular Weight: 441.33
EINECS: N/A
Product Categories: N/A
Mol File: 1174000-61-3.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: 4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide(1174000-61-3)
EPA Substance Registry System: 4-(methoxycarbonyl)-2,6-bis(4-(trifluoromethyl)phenyl)pyridine 1-oxide(1174000-61-3)

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: 1174000-61-3(Hazardous Substances Data)

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1174000-61-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1174000-61-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,4,0,0 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1174000-61:
(9*1)+(8*1)+(7*7)+(6*4)+(5*0)+(4*0)+(3*0)+(2*6)+(1*1)=103
103 % 10 = 3
So 1174000-61-3 is a valid CAS Registry Number.

1174000-61-3Upstream product

1174000-61-3Downstream Products

1174000-62-4 methyl 2,6-bis(4-(trifluoromethyl)phenyl)isonicotinate

1174000-61-3Relevant articles and documents

Direct arylation of azine N-oxides with aryl triflates

Schipper, Derek J.,El-Salfiti, Mohamed,Whipp, Christopher J.,Fagnou, Keith

experimental part, p. 4977 - 4983 (2009/10/17)

Palladium catalyzed direct arylation of azine N-oxides using aryl triflates to afford the corresponding 2-aryl azine N-oxides is described. The reaction is carried out with a range of both N-oxides and aryl triflates. The arylation can be carried out in s

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