Cas 55406-01-4,ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate

55406-01-4

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Basic information

Product Name: ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate
Synonyms: ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate
CAS NO:55406-01-4
Molecular Formula:
Molecular Weight: 401.388
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: ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate(55406-01-4)
EPA Substance Registry System: ethyl 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylate(55406-01-4)

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: 55406-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 55406-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,0 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55406-01:
(7*5)+(6*5)+(5*4)+(4*0)+(3*6)+(2*0)+(1*1)=104
104 % 10 = 4
So 55406-01-4 is a valid CAS Registry Number.

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55406-01-4Downstream Products

55914-58-4 4-methyl-2-phenyl-6-{[3-(trifluoromethyl)phenyl]amino}pyrimidine-5-carboxylic acid

55406-01-4Relevant academic research and scientific papers

Synthesis and antibacterial properties of pyrimidine derivatives

Cieplik, Jerzy,Stolarczyk, Marcin,Pluta, Janusz,Gubrynowicz, Olaf,Bryndal, Iwona,Lis, Tadeusz,Mikulewicz, Marcin

, p. 53 - 64 (2015/02/05)

In this study, a series of syntheses was conducted on the pyrimidine system, obtaining bisulfite carboxyl derivatives 4 and hydroxy derivatives 5. In addition, a series of syntheses were carried out as a result of which both alkyl and aromatic amines were

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