Cas 1313510-89-2,4-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine

1313510-89-2

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Basic information

Product Name: 4-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine
Synonyms: 4-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine
CAS NO:1313510-89-2
Molecular Formula:
Molecular Weight: 495.528
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-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine(1313510-89-2)
EPA Substance Registry System: 4-(3-fluorophenyl)-8-[(E)-(3-fluorophenyl)-methylidene]-3-(3-phenyl-1,2,4-oxadiazol-5-yl)-5,6,7,8-tetrahydro-4H-chromen-2-ylamine(1313510-89-2)

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: 1313510-89-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1313510-89-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,5,1 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1313510-89:
(9*1)+(8*3)+(7*1)+(6*3)+(5*5)+(4*1)+(3*0)+(2*8)+(1*9)=112
112 % 10 = 2
So 1313510-89-2 is a valid CAS Registry Number.

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1313510-89-2Relevant academic research and scientific papers

Antimycobacterial activity of novel 1,2,4-oxadiazole-pyranopyridine/ chromene hybrids generated by chemoselective 1,3-dipolar cycloadditions of nitrile oxides

Ranjith Kumar, Raju,Perumal, Subbu,Menéndez, J. Carlos,Yogeeswari, Perumal,Sriram, Dharmarajan

experimental part, p. 3444 - 3450 (2011/07/08)

The 1,3-dipolar cycloaddition of nitrile oxides generated in situ from benzohydroximinoyl chloride and triethylamine to 2-aminopyranopyridine-3- carbonitriles and 2-aminochromene-3-carbonitriles occurred chemoselectively furnishing novel 1,2,4-oxadiazole-

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