Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-

Base Information

Chemical Name:Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-
CAS No.:444811-13-6
Molecular Formula:C7H7BrN2O2
Molecular Weight:231.04700
Hs Code.:

Synonyms:ACETAMIDE,N-(5-BROMO-1,6-DIHYDRO-6-OXO-2-PYRIDINYL)-;N-(5-Bromo-6-oxo-1,6-dihydro-pyridin-2-yl)-acetamide;

Suppliers and Price of Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-

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

Labseeker
N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-acetamide 97
100g
$ 6125.00

Total 2 raw suppliers

Chemical Property of Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-

Chemical Property:

PSA：61.96000
LogP:1.16880

Purity/Quality:

98% ^*data from raw suppliers

N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-acetamide 97 ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-

There total 4 articles about Acetamide, N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)- 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:

: 444811-12-5
6-acetamido-3-bromopyridin-2-yl acetate

: 444811-13-6
N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-acetamide

Guidance literature:: With sodium hydroxide; In methanol; at 20 ℃; for 2h;
DOI:10.1016/S0040-4039(02)00481-1

Reference yield:

: 1072-97-5
5-bromo-2-pyridylamine

: 444811-13-6
N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-acetamide

Guidance literature:: Multi-step reaction with 4 steps

1: 2 h / 80 °C

2: m-chloroperbenzoic acid / CH₂Cl₂ / 20 °C

3: 60 - 80 °C

4: NaOH / methanol / 20 °C

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1002/anie.200602912

Reference yield:

: 7169-97-3
N-(5-bromopyridin-2-yl)acetamide

: 444811-13-6
N-(5-bromo-1,6-dihydro-6-oxo-2-pyridinyl)-acetamide

Guidance literature:: Multi-step reaction with 3 steps

1: m-chloroperbenzoic acid / CH₂Cl₂ / 20 °C

2: 60 - 80 °C

3: NaOH / methanol / 20 °C

With sodium hydroxide; 3-chloro-benzenecarboperoxoic acid; In methanol; dichloromethane;
DOI:10.1002/anie.200602912