Cas 371167-76-9,4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one

371167-76-9

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Basic information

Product Name: 4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one
Synonyms: 4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one
CAS NO:371167-76-9
Molecular Formula:
Molecular Weight: 330.359
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: 4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one(371167-76-9)
EPA Substance Registry System: 4-[2-(4-fluorophenyl)-1-morpholinoethylideneamino]-6-methyl-2H-pyran-2-one(371167-76-9)

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: 371167-76-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 371167-76-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,1,1,6 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 371167-76:
(8*3)+(7*7)+(6*1)+(5*1)+(4*6)+(3*7)+(2*7)+(1*6)=149
149 % 10 = 9
So 371167-76-9 is a valid CAS Registry Number.

371167-76-9Upstream product

371167-76-9Downstream Products

371167-76-9Relevant academic research and scientific papers

ν-Triazolines. Part 42. Study on the reactivity of 4,5-dihydro-1-(6-methyl-2-oxo-2H-pyran-4-yl)-5-morpholino-ν-triazoles. Synthetic approach to pyrano[4,3-b]pyrrol-4(1H)-ones

Erba,Pocar,Trimarco

, p. 1723 - 1728 (2007/10/03)

Pyrolysis of 4-aryl-5-morpholino-4,5-dihydrotriazoles 3 affords two products: pyrano[4,3-b]pyrrol-4(1H)-ones 4 and arylacetamidines 5. The reaction mechanism of this transformation is discussed and reaction conditions optimized to enhance the formation of

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