532134
2-Chloro-N-phenylacetamide
97%
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About This Item
Fórmula lineal:
C6H5NHCOCH2Cl
Número de CAS:
Peso molecular:
169.61
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
assay
97%
mp
136-139 °C (lit.)
functional group
amide
chloro
SMILES string
ClCC(=O)Nc1ccccc1
InChI
1S/C8H8ClNO/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,6H2,(H,10,11)
InChI key
VONWPEXRCLHKRJ-UHFFFAOYSA-N
General description
2-Chloro-N-phenylacetamide, also known as chloroacetanilide, can be prepared by reacting aniline with chloroacetylchloride in glacial acetic acid. The analysis of its crystal structure shows the presence of N-H...O hydrogen bonds between the molecules.
Application
2-Chloro-N-phenylacetamide may be used in the preparation of N,N′-(ethane-1,2-diyl)bis(2-(2-oxo-2-(phenylamino)ethoxy)benzamide), an amide podand. It may also be used to prepare phenylacetamide-based Schiff base ligands by reacting with corresponding hydrazones.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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J D Vargo
Analytical chemistry, 70(13), 2699-2703 (1998-07-17)
An analytical method is presented which permits qualitative and quantitative analysis of sulfonic acid degradates of three chloroacetanilide herbicides (acetochlor, alachlor, and metolachlor) and one chloroacetamide herbicide (dimethenamid) in groundwater at trace levels with determination by LC/MS/MS. The analytes were
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R E Biagini et al.
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Body burdens from exposures to pesticides may be estimated from urinary analyses of pesticide parent/metabolite concentrations. Pesticide applicators and others are often exposed to numerous unrelated pesticides, either sequentially or simultaneously. Classically, body burdens of pesticides are analyzed using chemical/instrumental
2-Chloro-N-phenylacetamide
Gowda BT, et al.
Acta Crystallographica Section E, Structure Reports Online, 64(6), o987-o987 (2008)
Synthesis and Fluorescence Properties of Eu3+, Tb3+ Complexes with Schiff Base Derivatives.
Liu Y, et al.
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