Cas 873948-86-8,Benzenesulfonamide, N,N'-[(4-amino-4H-1,2,4-triazole-3,5-diyl)bis(methylene)]bis[4-methyl-N -(2-pyridinylmethyl)-

873948-86-8

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Basic information

Product Name: Benzenesulfonamide, N,N'-[(4-amino-4H-1,2,4-triazole-3,5-diyl)bis(methylene)]bis[4-methyl-N -(2-pyridinylmethyl)-
Synonyms:
CAS NO:873948-86-8
Molecular Formula: C30H32N8O4S2
Molecular Weight: 632.767
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: Benzenesulfonamide, N,N'-[(4-amino-4H-1,2,4-triazole-3,5-diyl)bis(methylene)]bis[4-methyl-N -(2-pyridinylmethyl)-(CAS DataBase Reference)
NIST Chemistry Reference: Benzenesulfonamide, N,N'-[(4-amino-4H-1,2,4-triazole-3,5-diyl)bis(methylene)]bis[4-methyl-N -(2-pyridinylmethyl)-(873948-86-8)
EPA Substance Registry System: Benzenesulfonamide, N,N'-[(4-amino-4H-1,2,4-triazole-3,5-diyl)bis(methylene)]bis[4-methyl-N -(2-pyridinylmethyl)-(873948-86-8)

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: 873948-86-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 873948-86-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,9,4 and 8 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 873948-86:
(8*8)+(7*7)+(6*3)+(5*9)+(4*4)+(3*8)+(2*8)+(1*6)=238
238 % 10 = 8
So 873948-86-8 is a valid CAS Registry Number.

873948-86-8Upstream product

873948-86-8Downstream Products

873948-86-8Relevant academic research and scientific papers

Synthesis and some first-row transition-metal complexes of the 1,2,4-triazole-based bis(terdentate) ligands TsPMAT and PMAT

Klingele, Marco H.,Moubaraki, Boujemaa,Murray, Keith S.,Brooker, Sally

, p. 6962 - 6973 (2005)

The employment of a strategy based on nucleophilic substitution, rather than Schiff base condensation, for the preparation of 1,2,4-triazole-based ligands has been investigated and has led to the synthesis of two new ligands, 4-amino-3,5-bis{[N-(2-pyridyl

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