Cas 1147744-55-5,5-{[(4-phenyl-5-pyridin-4-yl-4H-1,2,4-triazol-3-yl)thio]methyl}-2(4-methylphenyl)-2-methylamino-1,3,4-thiadiazole

1147744-55-5

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Basic information

Product Name: 5-{[(4-phenyl-5-pyridin-4-yl-4H-1,2,4-triazol-3-yl)thio]methyl}-2(4-methylphenyl)-2-methylamino-1,3,4-thiadiazole
Synonyms:
CAS NO:1147744-55-5
Molecular Formula:
Molecular Weight: 471.61
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: 5-{[(4-phenyl-5-pyridin-4-yl-4H-1,2,4-triazol-3-yl)thio]methyl}-2(4-methylphenyl)-2-methylamino-1,3,4-thiadiazole(CAS DataBase Reference)
NIST Chemistry Reference: 5-{[(4-phenyl-5-pyridin-4-yl-4H-1,2,4-triazol-3-yl)thio]methyl}-2(4-methylphenyl)-2-methylamino-1,3,4-thiadiazole(1147744-55-5)
EPA Substance Registry System: 5-{[(4-phenyl-5-pyridin-4-yl-4H-1,2,4-triazol-3-yl)thio]methyl}-2(4-methylphenyl)-2-methylamino-1,3,4-thiadiazole(1147744-55-5)

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: 1147744-55-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1147744-55-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,7,7,4 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1147744-55:
(9*1)+(8*1)+(7*4)+(6*7)+(5*7)+(4*4)+(3*4)+(2*5)+(1*5)=165
165 % 10 = 5
So 1147744-55-5 is a valid CAS Registry Number.

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1147744-55-5Relevant academic research and scientific papers

Synthesis of some new 1,2,4-triazoles, their Mannich and Schiff bases and evaluation of their antimicrobial activities

Bayrak, Hacer,Demirbas, Ahmet,Karaoglu, Senguel Alpay,Demirbas, Neslihan

experimental part, p. 1057 - 1066 (2009/08/14)

4-Phenyl-5-pyridin-4-yl-4H-1,2,4-triazole-3-thiol (3) was obtained in basic media via the formation of 2-isonicotinoyl-N-phenylhydrazinecarbothioamide (2), and converted to some alkylated derivatives (4a,b) and Mannich base derivatives (5a-c). 2-[(4-Pheny

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