Cas 1456614-54-2,N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide

1456614-54-2

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Basic information

Product Name: N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide
Synonyms: N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide
CAS NO:1456614-54-2
Molecular Formula:
Molecular Weight: 406.446
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: N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide(1456614-54-2)
EPA Substance Registry System: N-(4-methyl-5-(4-(((2-nitrophenyl)amino)methyl)-5-thioxo-4,5-dihydro-1,3,4-oxadiazol-2-yl)thiazol-2-yl)acetamide(1456614-54-2)

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: 1456614-54-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1456614-54-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,6,6,1 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1456614-54:
(9*1)+(8*4)+(7*5)+(6*6)+(5*6)+(4*1)+(3*4)+(2*5)+(1*4)=172
172 % 10 = 2
So 1456614-54-2 is a valid CAS Registry Number.

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1456614-54-2Relevant academic research and scientific papers

Synthesis, antimicrobial and cytotoxic activities of some novel thiazole clubbed 1,3,4-oxadiazoles

Desai,Bhatt, Nayan,Somani, Hardik,Trivedi, Amit

, p. 54 - 59 (2013/10/01)

A series of thiazole clubbed 1,3,4-oxadiazole derivatives (5a-l) have been synthesized and characterized by IR, 1H NMR, 13C NMR and mass spectral analysis. Synthesized compounds were evaluated for their antimicrobial and cytotoxic ac

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