Cas 1217439-67-2,4-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde

1217439-67-2

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Basic information

Product Name: 4-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde
Synonyms: 4-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde
CAS NO:1217439-67-2
Molecular Formula:
Molecular Weight: 336.248
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-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 4-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde(1217439-67-2)
EPA Substance Registry System: 4-(1-(4-amino-2,3,5,6-tetrafluorophenyl)-1H-1,2,3-triazol-4-yl)benzaldehyde(1217439-67-2)

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: 1217439-67-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1217439-67-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,4,3 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1217439-67:
(9*1)+(8*2)+(7*1)+(6*7)+(5*4)+(4*3)+(3*9)+(2*6)+(1*7)=152
152 % 10 = 2
So 1217439-67-2 is a valid CAS Registry Number.

1217439-67-2Upstream product

1217439-66-1 (E)-4-azido-N-(4-ethynylbenzylidene)-2,3,5,6-tetrafluorobenzenamine

1217439-67-2Downstream Products

1217439-67-2Relevant academic research and scientific papers

Copper-free cycloaddition of azide and alkyne in crystalline state facilitated by arene-perfluoroarene interactions

Ni, Ben-Bo,Wang, Chong,Wu, Huixian,Pei, Jian,Ma, Yuguo

, p. 782 - 784 (2010)

Facilitated by arene-perfluoroarene interactions, a 1,3-dipolar cycloaddition between azide and alkyne proceeded in the crystals at room temperature in the absence of a copper(i) catalyst, and the reaction was confirmed to be a highly regioselective process giving the 1,4-triazole product.

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