N-(4-acetylphenyl)-2-bromoacetamide

Base Information

Chemical Name:N-(4-acetylphenyl)-2-bromoacetamide
CAS No.:29182-93-2
Molecular Formula:C₁₀H₁₀BrNO₂
Molecular Weight:256.099
Hs Code.:
DSSTox Substance ID:DTXSID701292168
Mol file:29182-93-2.mol

Synonyms:N-(4-acetylphenyl)-2-bromoacetamide;29182-93-2;SCHEMBL7687241;DTXSID701292168;MFCD02974382;STL570931;AKOS005172611;LS-03580

Suppliers and Price of N-(4-acetylphenyl)-2-bromoacetamide

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

Matrix Scientific
N-(4-Acetylphenyl)-2-bromoacetamide
1g
$ 258.00

Crysdot
N-(4-Acetylphenyl)-2-bromoacetamide 97%
5g
$ 527.00

Biosynth Carbosynth
N-(4-Acetylphenyl)-2-bromoacetamide
5 g
$ 578.00

Biosynth Carbosynth
N-(4-Acetylphenyl)-2-bromoacetamide
2 g
$ 289.00

Biosynth Carbosynth
N-(4-Acetylphenyl)-2-bromoacetamide
1 g
$ 170.00

Biosynth Carbosynth
N-(4-Acetylphenyl)-2-bromoacetamide
500 mg
$ 100.00

Biosynth Carbosynth
N-(4-Acetylphenyl)-2-bromoacetamide
250 mg
$ 57.50

AK Scientific
N-(4-Acetylphenyl)-2-bromoacetamide
500mg
$ 185.00

Total 2 raw suppliers

Chemical Property of N-(4-acetylphenyl)-2-bromoacetamide

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:254.98949
Heavy Atom Count:14
Complexity:222

Purity/Quality:

98%min ^*data from raw suppliers

N-(4-Acetylphenyl)-2-bromoacetamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)C1=CC=C(C=C1)NC(=O)CBr

Technology Process of N-(4-acetylphenyl)-2-bromoacetamide

There total 4 articles about N-(4-acetylphenyl)-2-bromoacetamide 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: 95.0%

: 99-92-3
p-aminobenzophenone

: 598-21-0
2-Bromoacetyl bromide

: 29182-93-2
N‐(4‐acetylphenyl)‐2‐bromoacetamide

Guidance literature:: With potassium carbonate; In dichloromethane; water; at 0 - 20 ℃;
DOI:10.1016/j.ejmech.2013.11.006

Reference yield:

: 99-92-3
p-aminobenzophenone

: 79-08-3
bromoacetic acid

: 29182-93-2
N‐(4‐acetylphenyl)‐2‐bromoacetamide

Guidance literature:: With 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 0 - 20 ℃;
DOI:10.1021/jm070564e

Reference yield:

: 62-53-3
aniline

: 29182-93-2
N‐(4‐acetylphenyl)‐2‐bromoacetamide

Guidance literature:: Multi-step reaction with 2 steps

1: zinc chloride / Verseifen des Reaktionsprodukts mit Salzsaeure

2: sodium acetate; aqueous acetic acid

With sodium acetate; acetic acid; zinc(II) chloride;