Cas 1463487-91-3,3-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole

1463487-91-3

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Basic information

Product Name: 3-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole
Synonyms: 3-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole
CAS NO:1463487-91-3
Molecular Formula:
Molecular Weight: 349.416
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-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole(1463487-91-3)
EPA Substance Registry System: 3-phenyl-5-methyl-6-(p-methoxyphenylazo)thiazolo[2,3-c][1,2,4]triazole(1463487-91-3)

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: 1463487-91-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1463487-91-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,6,3,4,8 and 7 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1463487-91:
(9*1)+(8*4)+(7*6)+(6*3)+(5*4)+(4*8)+(3*7)+(2*9)+(1*1)=193
193 % 10 = 3
So 1463487-91-3 is a valid CAS Registry Number.

1463487-91-3Upstream product

1270001-78-9 benzaldehyde N-(5-methoxyphenylazo-4-methylthiazol-2-yl)hydrazone

1463487-91-3Downstream Products

1463487-91-3Relevant academic research and scientific papers

New synthetic strategy for novel 6-arylazo-5-methyl-3-aryl-thiazolo[2,3-c]- [1,2,4]triazoles and study of their solvatochromic properties

Shawali, Ahmad Sami,Zayed, Mohie Eldin Moustafa

, p. 413 - 421 (2013/07/26)

Two series of 6-arylazothiazol[2,3- c ][1,2,4]triazoles were prepared via oxidative cyclization of the respective aldehyde N-(5-arylazo-4-methylthiazol-2- yl)-hydrazones. The structures of the latter hydrazone precursors and the azo compounds were confirm

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