Cas 1363250-76-3,3,3'-bis-(4-chlorobenzyl)-5,5'-bis-(p-tolyloxy)methyl-3H,3'H-[4,4']bi[[1,2,3]triazolyl]

1363250-76-3

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Basic information

Product Name: 3,3'-bis-(4-chlorobenzyl)-5,5'-bis-(p-tolyloxy)methyl-3H,3'H-[4,4']bi[[1,2,3]triazolyl]
Synonyms:
CAS NO:1363250-76-3
Molecular Formula:
Molecular Weight: 625.557
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: 3,3'-bis-(4-chlorobenzyl)-5,5'-bis-(p-tolyloxy)methyl-3H,3'H-[4,4']bi[[1,2,3]triazolyl](CAS DataBase Reference)
NIST Chemistry Reference: 3,3'-bis-(4-chlorobenzyl)-5,5'-bis-(p-tolyloxy)methyl-3H,3'H-[4,4']bi[[1,2,3]triazolyl](1363250-76-3)
EPA Substance Registry System: 3,3'-bis-(4-chlorobenzyl)-5,5'-bis-(p-tolyloxy)methyl-3H,3'H-[4,4']bi[[1,2,3]triazolyl](1363250-76-3)

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: 1363250-76-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1363250-76-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,3,2,5 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1363250-76:
(9*1)+(8*3)+(7*6)+(6*3)+(5*2)+(4*5)+(3*0)+(2*7)+(1*6)=143
143 % 10 = 3
So 1363250-76-3 is a valid CAS Registry Number.

1363250-76-3Upstream product

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1363250-76-3Relevant academic research and scientific papers

The use of glucose as alternative reducing agent in copper-catalyzed alkyne-azide cycloaddition

Garcia, Marco A.,Rios, Zita G.,Gonzalez, Jaime,Perez, Victor M.,Lara, Nancy,Fuentes, Aydee,Gonzalez, Carlos,Corona, David,Cuevas-Yanez, Erick

experimental part, p. 701 - 706 (2012/06/01)

1,2,3-triazoles were synthesized using several alkynes and azides as starting materials in the presence of glucose and catalytic amounts of Fehling reagent. This process is carried out under ambient pressure and temperature with good yields.

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