- Trityl Isocyanide as a Mechanistic Probe in Multicomponent Chemistry: Walking the Line between Ugi- and Strecker-type ReactionsCioc, Razvan C.; Preschel, Hans D.; van der Heijden, Gydo; Ruijter, Eelco ; Orru, Romano V. A., Chemistry - A European Journal, 2016, 22(23), 7837-7842
Cas no 1918941-25-9 (α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide)
1918941-25-9 structure
Product Name:α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide
CAS No:1918941-25-9
MF:C33H28N2O
MW:468.588228225708
CID:5667572
Update Time:2024-02-02
α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide Chemical and Physical Properties
Names and Identifiers
-
- α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide
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- Inchi: 1S/C33H28N2O/c36-32(31(26-16-6-1-7-17-26)34-30-24-14-5-15-25-30)35-33(27-18-8-2-9-19-27,28-20-10-3-11-21-28)29-22-12-4-13-23-29/h1-25,31,34H,(H,35,36)
- InChI Key: GBNAULGSRUAHHL-UHFFFAOYSA-N
- SMILES: C1(C(NC2=CC=CC=C2)C(NC(C2=CC=CC=C2)(C2=CC=CC=C2)C2=CC=CC=C2)=O)=CC=CC=C1
Experimental Properties
- Density: 1.180±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)
- Boiling Point: 702.9±60.0 °C(Predicted)
- pka: 12.93±0.46(Predicted)
α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide Production Method
Production Method 1
Reaction Conditions
1.1 Catalysts: p-Toluenesulfonic acid Solvents: Ethanol , Dichloromethane ; 1 h, rt
Reference
α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide Raw materials
α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide Preparation Products
α-(Phenylamino)-N-(triphenylmethyl)benzeneacetamide Related Literature
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Lei Yang,Yuan Zeng,Haibo Wu,Chunwu Zhou,Lei Tao J. Mater. Chem. B, 2020,8, 1383-1388
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
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James D. Kirkham,Patrick M. Delaney,George J. Ellames,Eleanor C. Row,Joseph P. A. Harrity Chem. Commun., 2010,46, 5154-5156
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