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Merck
CN

161659

4-Bromoacetanilide

98%

Synonym(s):

N-Acetyl-4-bromoaniline

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About This Item

Linear Formula:
CH3CONHC6H4Br
CAS Number:
103-88-8
Molecular Weight:
214.06
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24849944
EC Number:
203-154-9
Beilstein/REAXYS Number:
2208091
MDL number:
MFCD00000092
Assay:
98%
Form:
solid

Key Documents

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InChI key

MSLICLMCQYQNPK-UHFFFAOYSA-N

InChI

1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)

SMILES string

CC(=O)Nc1ccc(Br)cc1

assay

98%

form

solid

mp

165-169 °C (lit.)

solubility

alcohol: moderately soluble, benzene: soluble, chloroform: soluble, cold water: insoluble, ethyl acetate: soluble, water: very slightly soluble (hot)

functional group

amide, bromo

Quality Level

100

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General description

4-Bromoacetanilide is used as a building block in various organic transformations, including Suzuki and Heck reactions for the synthesis of pharmaceuticals.

Application

4-Bromoacetanilide was used as internal standard in determination of several phenylurea and triazine herbicides and their transformation products in oyster. It was used in the synthesis of new ligand for anchoring Gd(III) chelates onto TiO2 surface.

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
SDBB6301
SDBB2667
STBL0331
STBK7714
STBK6785

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1H NMR relaxivity of aqueous suspensions of titanium dioxide nanoparticles coated with a gadolinium (III) chelate of a DOTA-monoamide with a phenylphosphonate pendant arm.
Rehor I, et al.
Journal of Materials Chemistry, 19(10), 1494-1500 (2009)
Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines
Harris, Michele C, et al.
Organic Letters, 2885-2888 (2002)
E Bichon et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 838(2), 96-106 (2006-05-27)
A method was developed for the determination of several phenylurea and triazine herbicides and their transformation products in oysters at the low microg/kg level. Pressurised liquid extraction (PLE) of lyophilisated samples had required successive SPE combined with a liquid/liquid extraction

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