2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide

Base Information

Chemical Name:2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide
CAS No.:215649-75-5
Molecular Formula:C10H13 Br N2 O2
Molecular Weight:273.12642
Hs Code.:2924299090
DSSTox Substance ID:DTXSID80572417
Nikkaji Number:J985.825C
Wikidata:Q82460775
Mol file:215649-75-5.mol

Synonyms:215649-75-5;2-(2-HYDROXYETHYLAMINO)-N-(3-BROMOPHENYL)ACETAMIDE;N-(3-bromophenyl)-2-(2-hydroxyethylamino)acetamide;N-(3-Bromophenyl)-2-((2-hydroxyethyl)amino)acetamide;AB2865;DTXSID80572417;MFCD09037906;AKOS008958334;CS-0336427;A815481;N-(3-Bromophenyl)-N~2~-(2-hydroxyethyl)glycinamide

Suppliers and Price of 2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide

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

Crysdot
N-(3-Bromophenyl)-2-((2-hydroxyethyl)amino)acetamide 97%
5g
$ 353.00

Crysdot
N-(3-Bromophenyl)-2-((2-hydroxyethyl)amino)acetamide 97%
10g
$ 529.00

American Custom Chemicals Corporation
2-(2-HYDROXYETHYLAMINO)-N-(3-BROMOPHENYL)ACETAMIDE 95.00%
5MG
$ 503.40

AK Scientific
2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide
25g
$ 2064.00

Total 3 raw suppliers

Chemical Property of 2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide

Chemical Property:

PSA：61.36000
LogP:1.43340
XLogP3:1.2
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:272.01604
Heavy Atom Count:15
Complexity:202

Purity/Quality:

97% ^*data from raw suppliers

N-(3-Bromophenyl)-2-((2-hydroxyethyl)amino)acetamide 97% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Br)NC(=O)CNCCO

Technology Process of 2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide

There total 2 articles about 2-(2-Hydroxyethylamino)-N-(3-bromophenyl)acetamide 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: 66.0%

: 2564-03-6
[(3-bromophenyl)-aminocarbonylmethyl]chloride

: 141-43-5
ethanolamine

: 215649-75-5
N-(3-Bromo-phenyl)-2-(2-hydroxy-ethylamino)-acetamide

Guidance literature:: at 60 ℃; for 2h;
DOI:10.1016/S0040-4039(98)01670-0

Reference yield:

: 591-19-5
m-Bromoaniline

: 215649-75-5
N-(3-Bromo-phenyl)-2-(2-hydroxy-ethylamino)-acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: isopropyl acetate, aq. potassium bicarbonate / 0.5 h / 5 °C

2: 66 percent / 2 h / 60 °C

With Isopropyl acetate; potassium hydrogencarbonate;
DOI:10.1016/S0040-4039(98)01670-0

Reference yield: 88.0%

: 215649-75-5
N-(3-Bromo-phenyl)-2-(2-hydroxy-ethylamino)-acetamide

: 215649-81-3
1-(3-Bromo-phenyl)-piperazin-2-one; hydrochloride

Guidance literature:: With hydrogenchloride; tributylphosphine; di-tert-butyl-diazodicarboxylate; In ethyl acetate; 1.) 2 deg C to 5 deg C, 15 min; 2.) 40 deg C to 5 deg C, 1 h then 5 deg C, 1 h;
DOI:10.1016/S0040-4039(98)01670-0