2-(Bromomethyl)-5-methoxypyridine

Base Information

Chemical Name:2-(Bromomethyl)-5-methoxypyridine
CAS No.:209526-91-0
Molecular Formula:C7H8BrNO
Molecular Weight:202.04852
Hs Code.:
DSSTox Substance ID:DTXSID10462635
Nikkaji Number:J1.209.846D
Wikidata:Q82287196

Synonyms:2-(Bromomethyl)-5-methoxypyridine;209526-91-0;SCHEMBL5032709;2-Bromomethyl-5-methoxy-pyridine;DTXSID10462635;BWJMXVLESLHVNR-UHFFFAOYSA-N;AKOS016000724;SB21415;FT-0756638;O10507

Suppliers and Price of 2-(Bromomethyl)-5-methoxypyridine

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 2-(Bromomethyl)-5-methoxypyridine

Chemical Property:

XLogP3:1.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:200.97893
Heavy Atom Count:10
Complexity:99.6

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CN=C(C=C1)CBr

Technology Process of 2-(Bromomethyl)-5-methoxypyridine

There total 4 articles about 2-(Bromomethyl)-5-methoxypyridine 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:

: 127978-70-5
2-hydroxymethyl-5-methoxypyridine

: 209526-91-0
2-bromomethyl-5-methoxy-pyridine

Guidance literature:: With phosphorus tribromide; In dichloromethane; at 20 ℃; Cooling;

Reference yield:

: 1121-78-4
5-Hydroxy-2-methylpyridine

: 209526-91-0
2-bromomethyl-5-methoxy-pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: methanol; diethyl ether; toluene / 12.5 h / 20 °C / Inert atmosphere

2: N-Bromosuccinimide; dibenzoyl peroxide / benzene / 16 h / Inert atmosphere; Reflux

With N-Bromosuccinimide; dibenzoyl peroxide; In methanol; diethyl ether; toluene; benzene;
DOI:10.1021/jm2008369