Cas no 15935-94-1 (Allylidenetriphenylphosphorane)
15935-94-1 structure
Product Name:Allylidenetriphenylphosphorane
Allylidenetriphenylphosphorane Chemical and Physical Properties
Names and Identifiers
-
- Allylidenetriphenylphosphorane
- Triphenyl-2-propenylidenephosphorane
- Allylenetriphenylphosphorane
- Triphenylpropenylidenephosphorane
- Vinylmethylenetriphenylphosphorane
- allylidene(triphenyl)-$l^{5}-phosphane
- Phosphonium, allyltriphenyl-
- triphenyl(prop-2-enylidene)-lambda5-phosphane
- SCHEMBL7153777
- Triphenyl(prop-2-en-1-ylidene)-lambda~5~-phosphane
- Allyltriphenylphosphonium-
- Allylidenetriphenyl-l5-phosphane
- DTXSID10333290
- 15935-94-1
-
- Inchi： 1S/C21H19P/c1-2-18-22(19-12-6-3-7-13-19,20-14-8-4-9-15-20)21-16-10-5-11-17-21/h2-18H,1H2
- InChI Key： KTXDDSBSRMDZLM-UHFFFAOYSA-N
- SMILES： P(=CC=C)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1
Computed Properties
- Exact Mass: 302.12257
- Monoisotopic Mass: 302.122437604g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 0
- Heavy Atom Count: 22
- Rotatable Bond Count: 4
- Complexity: 338
- 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
- Surface Charge: 0
- Tautomer Count: nothing
- XLogP3: nothing
- Topological Polar Surface Area: 0?2
Experimental Properties
- Density: 1.09
- PSA: 0
Allylidenetriphenylphosphorane Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | A552603-5mg |
Allylidenetriphenylphosphorane |
15935-94-1 | 5mg |
$ 50.00 | 2022-06-08 | ||
| TRC | A552603-10mg |
Allylidenetriphenylphosphorane |
15935-94-1 | 10mg |
$ 65.00 | 2022-06-08 | ||
| TRC | A552603-50mg |
Allylidenetriphenylphosphorane |
15935-94-1 | 50mg |
$ 115.00 | 2022-06-08 |
Allylidenetriphenylphosphorane Related Literature
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1. Convenient synthesis of substituted cyclopentenones via [3?+?2] annulation of allylidenetriphenylphosphorane with 1,2-diacylethylenes: application to synthesis of (±)-methyl dehydrojasmonateYuichiro Himeda,Yasuhiro Tanaka,Ikuo Ueda,Minoru Hatanaka J. Chem. Soc. Perkin Trans. 1 1998 1389
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2. Intramolecular Diels–Alder reaction of 1-ethoxycarbonyl-4-alkenylcyclopentadienesYuichiro Himeda,Kazuhisa Hiratani,Minoru Hatanaka,Ikuo Ueda J. Chem. Soc. Chem. Commun. 1992 1684
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3. Heterocycles from ylides. Part III. Reactivity of allylic phosphonium ylides with 1,3-dipolesPiero Dalla Croce,Donato Pocar J. Chem. Soc. Perkin Trans. 1 1976 619
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4. Asymmetric synthesis of (+)-loline, a pyrrolizidine alkaloid from rye grass and tall fescuePaul R. Blakemore,Sung-Kee Kim,Volker K. Schulze,James D. White,Alexandre F. T. Yokochi J. Chem. Soc. Perkin Trans. 1 2001 1831
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5. Novel one-pot synthesis of 1-iodo-1-trimethylsilyl 1,3-dienesYanchang Shen,Tielin Wang,Wei Xia J. Chem. Soc. Perkin Trans. 1 1993 389
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