47712
Formanilide
purum, ≥98.0% (GC)
Synonym(s):
N-Phenylformamide
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About This Item
Linear Formula:
C6H5NHCHO
CAS Number:
Molecular Weight:
121.14
EC Number:
203-136-0
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
906934
MDL number:
grade
purum
assay
≥98.0% (GC)
bp
166 °C/14 mmHg (lit.)
mp
46-48 °C
density
1.144 g/mL at 25 °C (lit.)
SMILES string
O=CNc1ccccc1
InChI
1S/C7H7NO/c9-6-8-7-4-2-1-3-5-7/h1-6H,(H,8,9)
InChI key
DYDNPESBYVVLBO-UHFFFAOYSA-N
Storage Class
11 - Combustible Solids
wgk
WGK 2
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Regulatory Information
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Mitsuhiko Miyazaki et al.
Physical chemistry chemical physics : PCCP, 11(29), 6098-6106 (2009-07-17)
We measured the infrared (IR) spectra of supersonically cooled N-phenylformamide (formanilide) and N-phenylacetamide (acetanilide) in the amide band and X-H stretch vibration regions by using IR-UV depletion spectroscopy combined with a newly developed mid-IR light source based on difference frequency
Ahmed M Sh El-Sharief et al.
European journal of medicinal chemistry, 44(11), 4315-4334 (2009-08-12)
Halogenated and alkylated N-arylcyanothioformanilides were reacted with the nucleophilic reagents triethylamine, hydrazine and diphenyldiazomethane to produce N-arylcyanothioformanilide ammonium salts, a thiosemicarbazide and a 2-(arylamino)-3,3-diphenylacrylonitrile, respectively. They also underwent several types of electrophilic reactions with aryl-, arylbisisocyanates and arylisothiocyanates to yield
Johnson K Agbo et al.
The Journal of chemical physics, 127(6), 064315-064315 (2007-08-21)
A potential energy surface for trans-formanilide (TFA)-H2O is calculated and applied to study energy flow in the complex as well as the kinetics of water shuttling between hydrogen bonding sites on TFA. In addition to the previously identified H2O-TFA(C[Double Bond]O)
Aminolysis and hydrolysis of formanilide in water solutions. V. Influence of the substituent in para-position.
B Bergstrand
Acta pharmaceutica Suecica, 22(1), 1-16 (1985-01-01)
Xue-Bo Chen et al.
Journal of the American Chemical Society, 126(29), 8976-8980 (2004-07-22)
In the present study, the five lowest electronic states that control the UV photodissociation of formanilide and benzamide have been characterized using the complete active space self-consistent field theory. The mechanisms for the initial relaxation and subsequent dissociation processes have
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