Cas 1448959-48-5,2-{4-[(9H-fluoren-3-ylmethylene) amino]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N'-(phenylacetyl)acetohydrazide

1448959-48-5

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Product Name: 2-{4-[(9H-fluoren-3-ylmethylene) amino]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N'-(phenylacetyl)acetohydrazide
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CAS NO:1448959-48-5
Molecular Formula:
Molecular Weight: 480.526
EINECS: N/A
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Chemical Properties

Melting Point: N/A
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Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 2-{4-[(9H-fluoren-3-ylmethylene) amino]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N'-(phenylacetyl)acetohydrazide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{4-[(9H-fluoren-3-ylmethylene) amino]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N'-(phenylacetyl)acetohydrazide(1448959-48-5)
EPA Substance Registry System: 2-{4-[(9H-fluoren-3-ylmethylene) amino]-3-methyl-5-oxo-4,5-dihydro-1H-1,2,4-triazol-1-yl}-N'-(phenylacetyl)acetohydrazide(1448959-48-5)

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Hazardous Substances Data: 1448959-48-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1448959-48-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,9,5 and 9 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1448959-48:
(9*1)+(8*4)+(7*4)+(6*8)+(5*9)+(4*5)+(3*9)+(2*4)+(1*8)=225
225 % 10 = 5
So 1448959-48-5 is a valid CAS Registry Number.

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1448959-48-5Relevant academic research and scientific papers

Microwave-assisted synthesis of some 1H-1,2,4-triazol-3-one derivatives

Karaali, Nesrin,Mentese, Emre,Ylmaz, Fatih,Usta, Asu,Kahveci, Bahittin

, p. 72 - 76 (2013/07/26)

4-Amino-5-(methyl/ethyl)-2,4-dihydro-3H-1,2,4-triazol-3-one were synthesized from the reaction of (methyl/ethyl)-ester ethoxycarbonyl hydrazone with hydrazine hydrate and then, converted to corresponding Schiff bases using 9H-fluorene- 3-carbaldehyde. Ester, hydrazide and oxadiazole derivatives were synthesized starting from Schiff bases in three steps. All reactions occurred under conventional conditions and microwave irradiation. The obtained results were compared.

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