Cas 1373282-47-3,3-(4-((4-acetylphenylamino)methyl)-5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one

1373282-47-3

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Basic information

Product Name: 3-(4-((4-acetylphenylamino)methyl)-5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one
Synonyms:
CAS NO:1373282-47-3
Molecular Formula:
Molecular Weight: 451.573
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: 3-(4-((4-acetylphenylamino)methyl)-5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4-((4-acetylphenylamino)methyl)-5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one(1373282-47-3)
EPA Substance Registry System: 3-(4-((4-acetylphenylamino)methyl)-5-thioxo-4,5-dihydro-1,3,4-thiadiazol-2-yl)-1-ethyl-7-methyl-1,8-naphthyridin-4(1H)-one(1373282-47-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1373282-47-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1373282-47-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,7,3,2,8 and 2 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1373282-47:
(9*1)+(8*3)+(7*7)+(6*3)+(5*2)+(4*8)+(3*2)+(2*4)+(1*7)=163
163 % 10 = 3
So 1373282-47-3 is a valid CAS Registry Number.

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1373282-47-3Relevant academic research and scientific papers

Synthesis of Novel Nalidixic Acid-Based 1,3,4-Thiadiazole and 1,3,4-Oxadiazole Derivatives as Potent Antibacterial Agents

Aggarwal, Nisha,Kumar, Rajesh,Dureja, Prem,Khurana, Jitender Mohan

, p. 384 - 397 (2012)

Novel nalidixic acid-based 1,3,4-thia(oxa)diazoles, their thio ethers, sulfones, bis mercapto, and Mannich bases were synthesized and characterized by Infrared spectra, 1H NMR, 13C NMR, and elemental analysis. These compounds were ev

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