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161659

Sigma-Aldrich

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
Beilstein:
2208091
EC Number:
203-154-9
MDL number:
MFCD00000092
UNSPSC Code:
12352100
PubChem Substance ID:
24849944
NACRES:
NA.22

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)

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)

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