Cas 1224734-97-7,4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole

1224734-97-7

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Basic information

Product Name: 4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole
Synonyms: 4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole
CAS NO:1224734-97-7
Molecular Formula:
Molecular Weight: 542.615
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: 4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole(CAS DataBase Reference)
NIST Chemistry Reference: 4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole(1224734-97-7)
EPA Substance Registry System: 4-benzyl-5-(2-methoxyphenyl)-1-(4-methylphenylsulfonyl)-3-(4-nitrophenyl)-4,5-dihydro-1H-[1,2,4]triazole(1224734-97-7)

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: 1224734-97-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1224734-97-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,4,7,3 and 4 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1224734-97:
(9*1)+(8*2)+(7*2)+(6*4)+(5*7)+(4*3)+(3*4)+(2*9)+(1*7)=147
147 % 10 = 7
So 1224734-97-7 is a valid CAS Registry Number.

1224734-97-7Upstream product

1747-50-8 4-methyl-N'-[(4-nitrophenyl)methylidene]benzene-1-sulfonohydrazide

1224734-97-7Downstream Products

1224734-98-8 4-benzyl-3-(2-methoxyphenyl)-5-(4-nitrophenyl)-4H-[1,2,4]triazole

1224734-97-7Relevant academic research and scientific papers

Generation of azomethine imine and metal-free formal 1,3-dipolar cycloaddition of imine with PhIO: Reaction, scope, and synthesis

Maiti, Dilip K.,Chatterjee, Nirbhik,Pandit, Palash,Hota, Sandip K.

supporting information; experimental part, p. 2022 - 2024 (2010/09/10)

Generation of azomethine imine and its scope in regioselective 1,3-dipolar cycloaddition (DC) of imine with PhIO toward highly substituted Δ2-1,2,4-triazoline, 1,2,4-triazole, and their fused, chiral, and sugar-based analogues are demonstrated. The Royal Society of Chemistry.

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