1-Ethylpyridinium triflate

Base Information

• Chemical Name: 1-Ethylpyridinium triflate
• CAS No.: 3878-80-6
• Molecular Formula: CF₃O₃S*C₇H₁₀N
• Molecular Weight: 257.234
• European Community (EC) Number: 801-358-8
• ChEMBL ID: CHEMBL3185798
• DSSTox Substance ID: DTXSID9049291
• Mol file: 3878-80-6.mol

Synonyms:1-ethylpyridinium triflate;3878-80-6;DTXSID9049291;1-Ethylpyridinium trifluoromethanesulfonate;SCHEMBL1330325;CHEMBL3185798;DTXCID4029147;1-Ethylpyridinium triflate;99%;Tox21_202696;MFCD17014733;NCGC00260244-01;N-ethylpyridinium trifluoromethanesulfonate;CAS-3878-80-6;1-ethylpyridin-1-ium;trifluoromethanesulfonate

Chemical Property of 1-Ethylpyridinium triflate

Chemical Property:

• Density: 1.40 g/cm3 (24 °C)
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 1
• Exact Mass: 257.03334884
• Heavy Atom Count: 16
• Complexity: 200

Purity/Quality:

98% ^*data from raw suppliers

1-ETHYLPYRIDINIUM TRIFLATE 99.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: CC[N+]1=CC=CC=C1.C(F)(F)(F)S(=O)(=O)[O-]

Technology Process of 1-Ethylpyridinium triflate

There total 6 articles about 1-Ethylpyridinium triflate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

1-ethylpyridinium bromide (1906-79-2) + methyl trifluoromethanesulfonate (333-27-7) → N-ethylpyridinium trifluoromethanesulfonate (3878-80-6)

Guidance literature:

at 20 ℃; for 0.5h; Product distribution / selectivity;

Reference yield: 100.0%

trimethylsilyl trifluoromethanesulfonate (27607-77-8) + 1-ethylpyridinium bromide (1906-79-2) → N-ethylpyridinium trifluoromethanesulfonate (3878-80-6)

Guidance literature:

at 20 ℃; for 4h; Product distribution / selectivity;

Reference yield:

pyridine (110-86-1) + trifluorormethanesulfonic acid (1493-13-6) → pyridinium triflate (21179-04-4,52193-54-1) + N-ethylpyridinium trifluoromethanesulfonate (3878-80-6)

Guidance literature:

at 22 ℃; for 3h; Product distribution;

upstream raw materials:

pyridine

trifluorormethanesulfonic acid

1-ethylpyridinium bromide

methyl trifluoromethanesulfonate