2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine

Base Information

Chemical Name:2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine
CAS No.:688001-00-5
Molecular Formula:C9H10ClN3
Molecular Weight:
Hs Code.:
DSSTox Substance ID:DTXSID10435627
Wikidata:Q82250675

Synonyms:2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine;688001-00-5;SCHEMBL5748673;DTXSID10435627;LMJJZSPMCBFYNU-UHFFFAOYSA-N;FT-0762329;2-chloromethyl-3-ethyl 3h-imidazo[4,5-c]pyridine;2-(CHLOROMETHYL)-3-ETHYLIMIDAZO[4,5-C]PYRIDINE

Suppliers and Price of 2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine

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 4 raw suppliers

Chemical Property of 2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine

Chemical Property:

Vapor Pressure:0mmHg at 25°C
XLogP3:1.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:195.0563250
Heavy Atom Count:13
Complexity:176

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCN1C2=C(C=CN=C2)N=C1CCl

Technology Process of 2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine

There total 3 articles about 2-(chloromethyl)-3-ethyl-3H-imidazo[4,5-c]pyridine 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:

: 54-96-6
3,4-diaminopyridine

: 688001-00-5
2-chloromethyl-3-ethyl-3H-imidazo[4,5-c]pyridine

Guidance literature:: Multi-step reaction with 3 steps

1: 16 h / 20 - 22 °C

2: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 20 - 25 °C / Inert atmosphere

3: ethyl acetate / 16 h / Inert atmosphere

With lithium aluminium tetrahydride; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/op0502250

Reference yield:

: 676464-96-3
N-(4-aminopyridin-3-yl)acetamide hydrochloride

: 688001-00-5
2-chloromethyl-3-ethyl-3H-imidazo[4,5-c]pyridine

Guidance literature:: Multi-step reaction with 2 steps

1: lithium aluminium tetrahydride / tetrahydrofuran / 16 h / 20 - 25 °C / Inert atmosphere

2: ethyl acetate / 16 h / Inert atmosphere

With lithium aluminium tetrahydride; In tetrahydrofuran; ethyl acetate;
DOI:10.1021/op0502250