| Identification | Back Directory | [Name]
IODOMETHYL-TRIPHENYL-PHOSPHONIUM IODIDE
| [CAS]
3020-28-8 | [Synonyms]
NSC 116665
IodomethyL
-triphenyL
-phosphonium iodide
iodomethyl-triphenyl-phosphanium
iodo-(iodomethyl)-triphenylphosphorane
iodomethyl(triphenyl)phosphanium,iodide
Iodomethyl triphenylphosphonium iodide 95 %
(Iodomethyl)triphenylphosphonium iodide 95% | [Molecular Formula]
C19H17I2P | [MDL Number]
MFCD09025335 | [MOL File]
3020-28-8.mol | [Molecular Weight]
530.13 |
| Chemical Properties | Back Directory | [Melting point ]
260-266°C | [storage temp. ]
under inert gas (nitrogen or Argon) at 2–8 °C | [form ]
solid | [Appearance]
White to light yellow Solid | [InChI]
InChI=1S/C19H17IP.HI/c20-16-21(17-10-4-1-5-11-17,18-12-6-2-7-13-18)19-14-8-3-9-15-19;/h1-15H,16H2;1H/q+1;/p-1 | [InChIKey]
NAVMMSRRNOXQMJ-UHFFFAOYSA-M | [SMILES]
[P+](CI)(C1=CC=CC=C1)(C1=CC=CC=C1)C1=CC=CC=C1.[I-] |
| Hazard Information | Back Directory | [Uses]
Reactant or reagent for synthesis of:
- Phosphacyclic compounds via oxidative dimerizations
- Enamides via cross-coupling
- Cyclopeptide alkaloids for use as antibacterial or cytotoxic agents
- Terminal alkynes via dehydrohalogenation of aldehydes
Reactant for vinylcyclopropanation / cyclopentenation of strained alkenes using a sequential carborhodation process
Used as an olefination agent in the Lewis acid catalysis of electrocyclization of trienes | [reaction suitability]
reaction type: C-C Bond Formation |
|
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
China Langchem Inc.
|
| Telephone: |
0086-21-58956006 |
| Website: |
www.chemicalbook.com/ShowSupplierProductsList19141/0_EN.htm |
| Company Name: |
T&W GROUP
|
| Telephone: |
021-61551611 13296011611 |
| Website: |
www.trustwe.com/ |
|