Cas 407627-16-1,ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate

407627-16-1

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Basic information

Product Name: ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate
Synonyms: ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate
CAS NO:407627-16-1
Molecular Formula: C₂₀H₁₇N₅O₃
Molecular Weight: 375.38068
EINECS: N/A
Product Categories: N/A
Mol File: 407627-16-1.mol

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: /
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate(407627-16-1)
EPA Substance Registry System: ethyl 7-anilino-5-oxo-1-phenyl-1,5-dihydro[1,2,4]triazolo[4,3-a]pyrimidine-3-carboxylate(407627-16-1)

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: 407627-16-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 407627-16-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,0,7,6,2 and 7 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 407627-16:
(8*4)+(7*0)+(6*7)+(5*6)+(4*2)+(3*7)+(2*1)+(1*6)=141
141 % 10 = 1
So 407627-16-1 is a valid CAS Registry Number.

407627-16-1Upstream product

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407627-16-1Relevant academic research and scientific papers

Novel synthesis of 1,2,4-triazolo[4,3-a]pyrimidin-5-one derivatives

Hassaneen, Hamdi M,Abdelhadi, Hyam A,Abdallah, Tayseer A

, p. 10133 - 10138 (2007/10/03)

1,2-Dihydro-2-thioxopyrimidin-4(3H)ones 6 react with C-ethoxycarbonyl-N-arylhydrazonoyl chlorides 1 to give 1,2,4-triazolo[4,3-a]pyrimidines 11 in good yield. The latter products 11 react with benzenediazonium chloride, nitrous acid, acetyl chloride and chloroacetyl chloride to give the corresponding substitution products 16-18. The structures of the newly synthesized compounds are established on the basis of chemical and spectroscopic evidence.

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