Cas 1286706-53-3,1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole

1286706-53-3

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Basic information

Product Name: 1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole
Synonyms: 1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole
CAS NO:1286706-53-3
Molecular Formula:
Molecular Weight: 333.365
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: 1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole(1286706-53-3)
EPA Substance Registry System: 1-(4-fluorobenzyl)-4-((naphthalen-1-yloxy)methyl)-1H-1,2,3-triazole(1286706-53-3)

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: 1286706-53-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1286706-53-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,6,7,0 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1286706-53:
(9*1)+(8*2)+(7*8)+(6*6)+(5*7)+(4*0)+(3*6)+(2*5)+(1*3)=183
183 % 10 = 3
So 1286706-53-3 is a valid CAS Registry Number.

1286706-53-3Upstream product

1286706-53-3Downstream Products

1286706-53-3Relevant academic research and scientific papers

Click reactions catalyzed by Cu(I) complexes supported with dihydrobis(2-mercapto-benzimidazolyl)borate and phosphine ligands

Khalili, Dariush,Evazi, Roya,Neshat, Abdollah,Aboonajmi, Jasem,Osanlou, Farzane

supporting information, (2020/03/10)

Four Cu(I) complexes bearing dihydrobis(2-mercapto-benzimidazolyl)borate and phosphine co-ligands were synthesized and their catalytic activity was investigated in azide-alkyne reactions. These complexes were tested as catalyst system and among them a Cu(

Copper aluminate spinel in click chemistry: An efficient heterogeneous nanocatalyst for the highly regioselective synthesis of triazoles in water

Kavoosi, Leila,Khalafi-Nezhad, Ali,Khalili, Dariush

supporting information, p. 2136 - 2142 (2019/11/25)

An expeditious protocol for the one-pot synthesis of 1,4-disubstituted (β-hydroxy)-1,2,3-Triazoles in an aqueous medium has been developed using copper aluminate nanoparticles. This heterogeneous catalytic system was found to drive a multicomponent click reaction between organic azides (generated in situ from epoxides or halides) and terminal aliphatic or aromatic alkynes in up to 96percent yield without the need for a reducing agent. Structurally diverse 1,2,3-Triazoles were synthesized in good to excellent yields, and the catalyst could be easily separated by simple filtration, recycled, and reused in six subsequent cycles.

Click"-Capture, ring-opening metathesis polymerization (ROMP), release: Facile triazolation utilizing romp-derived oligomeric phosphates

Long, Toby R.,Faisal, Saqib,Maity, Pradip K.,Rolfe, Alan,Kurtz, Ryan,Klimberg, Sarra V.,Najjar, Uhammad-Rabbie,Basha, Fatima Z.,Hanson, Paul R.

supporting information; experimental part, p. 2038 - 2041 (2011/06/23)

Soluble, high-load ring-opening metathesis polymerization (ROMP)-derived oligomeric triazole phosphates (OTP) are reported for application as efficient triazolating reagents of nucleophilic species. Utilizing a "Click"- capture, ROMP, release protocol, th

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