Cas 428480-06-2,5-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol

428480-06-2

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Basic information

Product Name: 5-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol
Synonyms: 5-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol
CAS NO:428480-06-2
Molecular Formula:
Molecular Weight: 348.351
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-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol(CAS DataBase Reference)
NIST Chemistry Reference: 5-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol(428480-06-2)
EPA Substance Registry System: 5-phenyl-4-{[2-(trifluoromethyl)benzylidene]amino}-4H-1,2,4-triazole-3-thiol(428480-06-2)

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: 428480-06-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 428480-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,8,4,8 and 0 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 428480-06:
(8*4)+(7*2)+(6*8)+(5*4)+(4*8)+(3*0)+(2*0)+(1*6)=152
152 % 10 = 2
So 428480-06-2 is a valid CAS Registry Number.

428480-06-2Upstream product

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428480-06-2Relevant academic research and scientific papers

Thiosemicarbazone fragment embedded within 1,2,4-triazole ring as inhibitors of Entamoeba histolytica

Siddiqui, Shadab Miyan,Salahuddin, Attar,Azam, Amir

, p. 2768 - 2771 (2012)

A series of 1,2,4-triazole derivatives containing thiosemicarbazone linkage was synthesized and evaluated for their in vitro antiamoebic activity against HM1:IMSS strain of Entamoeba histolytica. All the compounds were capable of inhibiting the growth of

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