Cas 1320264-34-3,3-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole

1320264-34-3

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Basic information

Product Name: 3-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole
Synonyms: 3-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole
CAS NO:1320264-34-3
Molecular Formula:
Molecular Weight: 259.224
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-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole(CAS DataBase Reference)
NIST Chemistry Reference: 3-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole(1320264-34-3)
EPA Substance Registry System: 3-(4'-nitrobenzoyl)-5,6-dihydro-4H-imidazo[1,2-c][1,2,3]triazole(1320264-34-3)

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: 1320264-34-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1320264-34-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,0,2,6 and 4 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1320264-34:
(9*1)+(8*3)+(7*2)+(6*0)+(5*2)+(4*6)+(3*4)+(2*3)+(1*4)=103
103 % 10 = 3
So 1320264-34-3 is a valid CAS Registry Number.

1320264-34-3Upstream product

124927-43-1 2-(4-nitrobenzoylmethylene)imidazolidine

1320264-34-3Downstream Products

1320264-34-3Relevant academic research and scientific papers

Facile and quantitative synthesis of 1,3-diazaheterocycle-fused 1,2,3-triazole derivatives using fluoroalkanesulfonyl azide as a diazo transfer reagent

Gu, Jiwei,Xiong, Wanting,Zhang, Zhenhua,Zhu, Shizheng

, p. 1717 - 1722 (2011)

A series of 1,3-diazaheterocycle-fused 1,2,3-triazoles were conveniently and quantitatively prepared by 1,3-dipolar cycloaddition of heterocyclic ketene aminals with fluoroalkanesulfonyl azide, followed by elimination of fluoroalkanesulfonyl amide at room

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