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Methyltriphenylphosphonium iodide_Molecular_structure_CAS_2065-66-9)
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Methyltriphenylphosphonium iodide

Catalog No. 245054 Name Sigma Aldrich
CAS Number 2065-66-9 Website http://www.sigmaaldrich.com
M. F. C19H18IP Telephone 1-800-521-8956
M. W. 404.224451 Fax
Purity 97% Email
Storage Chembase ID: 80955

SYNONYMS

Title
甲基三苯基碘化膦
IUPAC name
methyltriphenylphosphanium iodide
IUPAC Traditional name
methyltriphenylphosphanium iodide

DATABASE IDS

EC Number 218-178-5
MDL Number MFCD00066175
PubChem SID 24854729
CAS Number 2065-66-9

PROPERTIES

Linear Formula CH3P(C6H5)3I
Purity 97%
Melting Point 183-185 °C(lit.)
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3

DETAILS

Description (English)
Packaging
25 g in glass bottle
Legal Information
Product of Fluorous Technologies, Inc.
Application
Reactant for synthesis of:
• Triphenylamine-based dyes1 and polyolefinic aromatic molecules with pyrene2 for use in dye-sensitized solar cells
• Diastereoisomeric carba analogs of glycal-derived vinyl epoxides for the production of carbasugars3
• Alkaloid natural products via organocascade catalysis4
• Triplet carbenes via oxidation of allene compounds5
• Stilbenes via dehydrohalogenation-Heck olefination and Wittig-Heck reactions6
Description (简体中文)
包装
25 g in glass bottle
Legal Information
Fluorous Technologies, Inc. 产品。该化合物的使用受美国专利 6,156,896、5,859,247、5,777,121 和 6,673,539 的保护。
Application
Reactant for synthesis of:
• Triphenylamine-based dyes1 and polyolefinic aromatic molecules with pyrene2 for use in dye-sensitized solar cells
• Diastereoisomeric carba analogs of glycal-derived vinyl epoxides for the production of carbasugars3
• Alkaloid natural products via organocascade catalysis4
• Triplet carbenes via oxidation of allene compounds5
• Stilbenes via dehydrohalogenation-Heck olefination and Wittig-Heck reactions6

REFERENCES