甲酰苯胺
甲酰苯胺结构式
|
常用名 | 甲酰苯胺 | 英文名 | Formamide, N-phenyl- |
|---|---|---|---|---|
| CAS号 | 103-70-8 | 分子量 | 121.13700 | |
| 密度 | 1.144 g/mL at 25 °C(lit.) | 沸点 | 166 °C14 mm Hg(lit.) | |
| 分子式 | C7H7NO | 熔点 | 46-48 °C(lit.) | |
| MSDS | 美版 | 闪点 | >230 °F |
|
ZEKE photoelectron spectroscopy of the cis and trans isomers of formanilide.
Angew. Chem. Int. Ed. Engl. 41(1) , 166-8, (2002)
|
|
|
Phosphazene base-catalyzed condensation of trimethylsilylacetate with carbonyl compounds.
Chem. Commun. (Camb.) (29) , 3128-30, (2006) The t-Bu-P4 base was found to be an excellent catalyst for the condensation of trimethylsilylacetate or trimethylacetonitrile with carbonyl compounds to form functionalized alkenes and beta-enaminoesters were also synthesized by the condensation with formanil... |
|
|
Isomer selective infrared spectroscopy of supersonically cooled cis- and trans-N-phenylamides in the region from the amide band to NH stretching vibration.
Phys. Chem. Chem. Phys. 11(29) , 6098-106, (2009) 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... |
|
|
Direct calculation of electron transfer parameters through constrained density functional theory.
J. Phys. Chem. A 110(29) , 9212-8, (2006) It is shown that constrained density functional theory (DFT) can be used to access diabatic potential energy surfaces in the Marcus theory of electron transfer, thus providing a means to directly calculate the driving force and the inner-sphere reorganization... |
|
|
Insights into photodissociation dynamics of benzamide and formanilide from ab initio calculations.
J. Am. Chem. Soc. 126(29) , 8976-80, (2004) 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 subs... |
|
|
Synthesis, characterization and derivatization of some novel types of mono- and bis-imidazolidineiminothiones and imidazolidineiminodithiones with antitumor, antiviral, antibacterial and antifungal activities – part I
Eur. J. Med. Chem. 44(11) , 4315-34, (2009) 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-diphenylacryl... |
|
|
Aminolysis and hydrolysis of formanilide in water solutions. V. Influence of the substituent in para-position.
Acta Pharm. Suec. 22(1) , 1-16, (1985)
|
|
|
Quantum energy flow and the kinetics of water shuttling between hydrogen bonding sites on trans-formanilide.
J. Chem. Phys. 127(6) , 064315, (2007) 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[Doubl... |
|
|
Hydration of a cationic amide group: a ZEKE spectroscopic study of trans-formanilide-H2O. Ullrich S, et al.
Phys. Chem. Chem. Phys. 4(13) , 2897-2903, (2002)
|