Cas no 38821-11-3 (2-(triphenyl-lambda~5~-phosphanylidene)acetamide)
38821-11-3 structure
Product Name:2-(triphenyl-lambda~5~-phosphanylidene)acetamide
CAS No:38821-11-3
MF:C20H18NOP
MW:319.336785793304
CID:1491573
PubChem ID:38099
Update Time:2025-04-21
2-(triphenyl-lambda~5~-phosphanylidene)acetamide Chemical and Physical Properties
Names and Identifiers
-
- 2-(triphenyl-lambda~5~-phosphanylidene)acetamide
- 2-(triphenyl-λ<sup>5</sup>-phosphanylidene)acetamide
- Phosphonium, triphenyl-, carbamoylmethylide
- 2-(triphenyl-lambda5-phosphanylidene)acetamide
- ACETAMIDE, 2-(TRIPHENYLPHOSPHORANYLIDENE)-
- DTXSID30192083
- BRN 0803830
- 2-(Triphenylphosphoranylidene)acetamide
- SCHEMBL5694513
- 38821-11-3
- carbamoylmethylene triphenylphosphorane
- carbamoylmethylene-triphenylphosphorane
- Triphenylphosphonium carbamoylmethylide
- NKFMHVSOHCEONZ-UHFFFAOYSA-N
- (Triphenylphosphoranylidene)acetamide
-
- Inchi： 1S/C20H18NOP/c21-20(22)16-23(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19/h1-16H,(H2,21,22)
- InChI Key： NKFMHVSOHCEONZ-UHFFFAOYSA-N
- SMILES： P(=CC(N)=O)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1
Computed Properties
- Exact Mass: 319.11274
- Monoisotopic Mass: 319.113
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 23
- Rotatable Bond Count: 4
- Complexity: 388
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 43.1A^2
- XLogP3: 3
Experimental Properties
- Density: 1.2
- Boiling Point: 507.8°C at 760 mmHg
- Flash Point: 260.9°C
- Refractive Index: 1.638
- PSA: 43.09
- LogP: 2.96830
2-(triphenyl-lambda~5~-phosphanylidene)acetamide Related Literature
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
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Denis V. Korchagin,Elena A. Yureva,Alexander V. Akimov,Eugenii Ya. Misochko,Gennady V. Shilov,Artem D. Talantsev,Roman B. Morgunov,Alexander A. Shakin,Sergey M. Aldoshin,Boris S. Tsukerblat Dalton Trans., 2017,46, 7540-7548
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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Ana G. Neo,Ana Bornadiego,Jesús Díaz,Stefano Marcaccini,Carlos F. Marcos Org. Biomol. Chem., 2013,11, 6546-6555
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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