추천 제품
Quality Level
분석
99%
양식
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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애플리케이션
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
개인 보호 장비
Eyeshields, Gloves, type N95 (US)
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)
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)
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)
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)
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
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