Acetanilide

Acetanilide is an aniline derivative. Crystal structure of acetanillide has been studied by X-ray diffraction. It crystallizes in orthorhombic system having space group of Pbca. Its photolysis has been studied in the presence of β-cyclodextrin (cycloheptaamylose). Aminoacetophenone derivatives are obtained by the Fries rearrangement of acetanilide in the presence zeolites Y and β.

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Catalog Number CBB1111322
Alternative Name(s) N-Phenylacetamide
Molecular Formula CH3CONHC6H5
CAS# 103-84-4
Purity >99%
Inchi 1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)
Inchi Key FZERHIULMFGESH-UHFFFAOYSA-N
SMILES CC(=O)Nc1ccccc1
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Acetanilide

Pd(OAc)2 and Cu(OAc)2 catalyzed regioselective C-H functionalization/halogenation of acetanilide has been reported to afford ortho-haloacetanilides. Crystal structure of acetanilide has been studied by X-ray diffraction. Photorearrangement of acetanilide has been studied in the presence of β-cyclodextrin (cycloheptaamylose). Two-color REMPI (resonance enhanced multiphoton ionization) and ZEKE (zero kinetic energy photoelectron) spectra of the trans-acetanilide·H2O complex has been reported. Femtosecond IR spectroscopy of delocalized NH excitations of crystalline acetanilide has been studied. Fries rearrangement of acetanilide over zeolites Y and Beta affords corresponding aminoacetophenones.

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Catalog Number CBB1111323
Alternative Name(s) N-Phenylacetamide
Molecular Formula CH3CONHC6H5
CAS# 103-84-4
Purity >99%
Inchi 1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)
Inchi Key FZERHIULMFGESH-UHFFFAOYSA-N
SMILES CC(=O)Nc1ccccc1
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Acetanilide

Acetanilide undergoes palladium-catalyzed cross-coupling reaction to form ortho-acylacetanilide.

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Catalog Number CBB1111325
Alternative Name(s) N-Phenylacetamide
Molecular Formula CH3CONHC6H5
CAS# 103-84-4
Purity >99%
Inchi 1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)
Inchi Key FZERHIULMFGESH-UHFFFAOYSA-N
SMILES CC(=O)Nc1ccccc1
Size Inquiry
Supplier Page https://www.amerigoscientific.com/acetanilide-item-111325.html