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Sigma-Aldrich

Formanilide

99%

Synonym(s):

N-Phenylformamide

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About This Item

Linear Formula:
C6H5NHCHO
CAS Number:
103-70-8
Molecular Weight:
121.14
Beilstein:
906934
EC Number:
203-136-0
MDL number:
MFCD00003276
UNSPSC Code:
12352100
PubChem Substance ID:
24848101
NACRES:
NA.22

Assay

99%

form

powder

bp

166 °C/14 mmHg (lit.)

mp

46-48 °C (lit.)

solubility

water: soluble 25.4 g/L at 20 °C
water: soluble 28.6 g/L at 25 °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

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Application

Formanilide was used to study the zero electron kinetic energy(ZEKE) spectra of cis- and trans-formanilide. It was used to investigate the gas-phase structures of the two isomers of the trans-formanilide-water complex by two-colour (1+1′) resonance enhanced multiphoton ionisation (REMPI) and ZEKE spectroscopy.

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

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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Hydration of a cationic amide group: a ZEKE spectroscopic study of trans-formanilide-H2O.
Ullrich S, et al.
Physical Chemistry Chemical Physics, 4(13), 2897-2903 (2002)
ZEKE photoelectron spectroscopy of the cis and trans isomers of formanilide.
Susanne Ullrich et al.
Angewandte Chemie (International ed. in English), 41(1), 166-168 (2002-12-20)
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)
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
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
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