2-[(4-bromophenoxy)methyl]-1H-benzimidazole

Base Information

Chemical Name:2-[(4-bromophenoxy)methyl]-1H-benzimidazole
CAS No.:3156-20-5
Molecular Formula:C₁₄H₁₁BrN₂O
Molecular Weight:303.158
Hs Code.:
DSSTox Substance ID:DTXSID301320262
ChEMBL ID:CHEMBL171325

Synonyms:2-[(4-bromophenoxy)methyl]-1H-benzimidazole;3156-20-5;CHEMBL171325;MLS001176986;DTXSID301320262;HMS2881P14;BDBM50404916;AKOS005202891;SMR000589262;CS-0220276;EN300-06251;2-[(4-bromophenoxy)methyl]-1H-1,3-benzodiazole;SR-01000044015;SR-01000044015-1;2-(4-BROMOPHENOXYMETHYL)-1H-1,3-BENZODIAZOLE;Z55692981

Suppliers and Price of 2-[(4-bromophenoxy)methyl]-1H-benzimidazole

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 5 raw suppliers

Chemical Property of 2-[(4-bromophenoxy)methyl]-1H-benzimidazole

Chemical Property:

XLogP3:3.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:302.00548
Heavy Atom Count:18
Complexity:269

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C2C(=C1)NC(=N2)COC3=CC=C(C=C3)Br

Technology Process of 2-[(4-bromophenoxy)methyl]-1H-benzimidazole

There total 1 articles about 2-[(4-bromophenoxy)methyl]-1H-benzimidazole 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:

: 1878-91-7
(4-bromophenoxy)acetic acid

: 95-54-5
1,2-diamino-benzene

: 3156-20-5
2-(4-bromo-phenoxymethyl)-1H-benzoimidazole

Guidance literature:: With hydrogenchloride; Heating;
DOI:10.1021/jm00350a002

Reference yield: 87.0%

: 3156-20-5
2-(4-bromo-phenoxymethyl)-1H-benzoimidazole

: 107-07-3
2-chloro-ethanol

: C₁₆H₁₅BrN₂O₂

Guidance literature:: With tetrabutylammomium bromide; sodium hydroxide; In acetone; at 65 ℃; for 5h;

Reference yield:

: 3156-20-5
2-(4-bromo-phenoxymethyl)-1H-benzoimidazole

: C₂₉H₂₅BrN₂O₉

Guidance literature:: Multi-step reaction with 2 steps

1: tetrabutylammomium bromide; sodium hydroxide / acetone / Reflux

2: triethylamine / dichloromethane / 10 h / 25 °C / Cooling with ice

With tetrabutylammomium bromide; triethylamine; sodium hydroxide; In dichloromethane; acetone;