1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide

Base Information

Chemical Name:1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide
CAS No.:366-61-0
Molecular Formula:Br*C₁₄H₁₃FNO
Molecular Weight:310.166
Hs Code.:
DSSTox Substance ID:DTXSID90957872
NSC Number:34174
Mol file:366-61-0.mol

Synonyms:366-61-0;1-(4-fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide;SCHEMBL3884195;DTXSID90957872;NSC34174;NSC-34174;AKOS024330923;1-[2-(4-Fluorophenyl)-2-oxoethyl]-2-methylpyridin-1-iumato bromido

Suppliers and Price of 1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of 1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide

Chemical Property:

Vapor Pressure:8.09E-06mmHg at 25°C
Boiling Point:374.9°C at 760 mmHg
Flash Point:180.5°C
Density:1.126g/cm³
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:309.01645
Heavy Atom Count:18
Complexity:261

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=CC=[N+]1CC(=O)C2=CC=C(C=C2)F.[Br-]

Technology Process of 1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide

There total 1 articles about 1-(4-Fluorophenyl)-2-(2-methylpyridin-1-ium-1-yl)ethanone;bromide 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: 80.0%

: 109-06-8
α-picoline

: 403-29-2
2-bromo-4'-fluoroacetophenone

: 366-61-0
1-(4-fluoro-phenacyl)-2-methyl-pyridinium; bromide

Guidance literature:: Heating;

Reference yield: 29.8%

: 366-61-0
1-(4-fluoro-phenacyl)-2-methyl-pyridinium; bromide

: 7607-48-9
2-(4-fluorophenyl)indolizine

Guidance literature:: With potassium hydrogencarbonate; In water; for 1h; Heating;

Reference yield:

: 366-61-0
1-(4-fluoro-phenacyl)-2-methyl-pyridinium; bromide

: 2-(4-fluoro-phenyl)-3-nitroso-indolizine

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous sodium hydrogencarbonate solution

2: aqueous hydrochloric acid; sodium nitrite

With hydrogenchloride; sodium hydrogencarbonate; sodium nitrite;