161659
4-Bromoacetanilide
98%
Synonym(s):
N-Acetyl-4-bromoaniline
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About This Item
Linear Formula:
CH3CONHC6H4Br
CAS Number:
Molecular Weight:
214.06
Beilstein:
2208091
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
SMILES string
CC(=O)Nc1ccc(Br)cc1
InChI
1S/C8H8BrNO/c1-6(11)10-8-4-2-7(9)3-5-8/h2-5H,1H3,(H,10,11)
InChI key
MSLICLMCQYQNPK-UHFFFAOYSA-N
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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 Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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.
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Improved functional group compatibility in the palladium-catalyzed synthesis of aryl amines
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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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