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Merck

00401

Acetanilide

puriss. p.a., ≥99.5% (CHN)

Synonyme(s) :

N-Phenylacetamide

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A propos de cet article

Formule linéaire :
CH3CONHC6H5
Numéro CAS:
Poids moléculaire :
135.16
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39031308
UNSPSC Code:
12352100
EC Number:
203-150-7
MDL number:
Beilstein/REAXYS Number:
606468
Assay:
≥99.5% (CHN)
Form:
solid
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vapor density

4.65 (vs air)

Quality Level

vapor pressure

1 mmHg ( 114 °C)

grade

puriss. p.a.

assay

≥99.5% (CHN)

form

solid

autoignition temp.

1004 °F

bp

304 °C (lit.)

mp

113-115 °C

functional group

amide

SMILES string

CC(=O)Nc1ccccc1

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

General description

Acetanilide is a member of acetamides. It is used as a precursor compound in the synthesis of dyes, varnishes, and rubber accelerators. It is also used as a key intermediate for many pharmaceutical compounds.

Application

Acetanilide can be used as a reactant to synthesize:      
  • Oxindole derivatives via Ir-catalyzed intermolecular C-H functionalization with diazotized Meldrum′s acid.     
  • Ortho-Haloacetanilides via regioselective C-H functionalization/halogenation reaction in the presence of Pd(OAc)2 and Cu(OAc)2 catalyst.      
  • Chlorosubstituted acetanilides via oxidative chlorination with HCI and m-chloroperbenzoic acid in DMF.



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hcodes

Hazard Classifications

Acute Tox. 4 Oral

Classe de stockage

11 - Combustible Solids

wgk

WGK 1

flash_point_f

321.8 °F - closed cup

flash_point_c

161 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves



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Fabrice Gritti et al.
Journal of chromatography. A, 1355, 179-192 (2014-07-09)
The mass transfer mechanism in four prototype columns (2.1 and 3.0×50mm, 2.1 and 3.0×100mm) packed with 1.9μm fully porous Titan-C18 particles was investigated by using two previously reported home-made protocols. The first one was used to measure the eddy dispersion
Naoki Aizawa et al.
Neurourology and urodynamics, 34(4), 368-374 (2014-02-18)
We measured single-unit mechanosensitive afferent activities (SAAs) during reflexic, rhythmic bladder contractions (RBCs), and examined whether L-arginine, an NO substrate, and mirabegron, a β3-adrenoceptor agonist, and oxybutynin, an antimuscarinic agent, can affect the SAAs in such condition. Twenty-nine female Sprague-Dawley
Hassan A Alhazmi et al.
Journal of pharmaceutical and biomedical analysis, 107, 311-317 (2015-02-02)
In this work, the behavior of several metal ions with different globular proteins was investigated by affinity capillary electrophoresis. Screening was conducted by applying a proper rinsing protocol developed by our group. The use of 0.1M EDTA in the rinsing