5-bromo-N-(4-bromophenyl)pentanamide

Base Information

Chemical Name:5-bromo-N-(4-bromophenyl)pentanamide
CAS No.:948883-07-6
Molecular Formula:C₁₁H₁₃Br₂NO
Molecular Weight:335.038
Hs Code.:
DSSTox Substance ID:DTXSID70704664
Wikidata:Q82637146
Mol file:948883-07-6.mol

Synonyms:5-bromo-N-(4-bromophenyl)pentanamide;948883-07-6;SCHEMBL4654699;DTXSID70704664;DEBXWAMSKVXSKM-UHFFFAOYSA-N;FT-0717346

Suppliers and Price of 5-bromo-N-(4-bromophenyl)pentanamide

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 1 raw suppliers

Chemical Property of 5-bromo-N-(4-bromophenyl)pentanamide

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:334.93434
Heavy Atom Count:15
Complexity:191

Purity/Quality:: 97% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC=C1NC(=O)CCCCBr)Br

Technology Process of 5-bromo-N-(4-bromophenyl)pentanamide

There total 2 articles about 5-bromo-N-(4-bromophenyl)pentanamide 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: 99.0%

: 4509-90-4
5-bromovaleroyl chloride

: 106-40-1
4-bromo-aniline

: 948883-07-6
5-bromo-N-(4-bromophenyl)pentanamide

Guidance literature:: With triethylamine; In dichloromethane; at 0 ℃; for 3h;

Reference yield:

: 2067-33-6
5-bromopentanoic acid

: 948883-07-6
5-bromo-N-(4-bromophenyl)pentanamide

Guidance literature:: Multi-step reaction with 2 steps

1: oxalyl dichloride / 0.75 h / 20 °C / Inert atmosphere

2: triethylamine / dichloromethane / 1 h / -78 - 20 °C / Inert atmosphere

With oxalyl dichloride; triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2012.02.052

Reference yield: 85.0%

: 110-91-8,99108-56-2
morpholine

: 948883-07-6
5-bromo-N-(4-bromophenyl)pentanamide

: 874449-07-7
5-(morpholin-4-yl)pentanoic acid (4-bromophenyl)amide

Guidance literature:: With triethylamine; sodium iodide; In N,N-dimethyl-formamide; for 16h; Reflux; Inert atmosphere;
DOI:10.1016/j.bmcl.2012.02.052