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(Ethoxycarbonylmethyl)triphenylphosphonium chloride_Molecular_structure_CAS_17577-28-5)
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(Ethoxycarbonylmethyl)triphenylphosphonium chloride

Catalog No. 02615 Name Sigma Aldrich
CAS Number 17577-28-5 Website http://www.sigmaaldrich.com
M. F. C22H22ClO2P Telephone 1-800-521-8956
M. W. 384.835641 Fax
Purity ≥90% (AT) Email
Storage Chembase ID: 74862

SYNONYMS

Title
(乙氧基羰基甲基)三苯基氯化膦
IUPAC name
(2-ethoxy-2-oxoethyl)triphenylphosphanium chloride
IUPAC Traditional name
(2-ethoxy-2-oxoethyl)triphenylphosphanium chloride
Synonyms
(2-Ethoxy-2-oxoethyl)triphenylphosphonium chloride

DATABASE IDS

MDL Number MFCD00011746
PubChem SID 24845340
Beilstein Number 3924139
EC Number 241-548-2
CAS Number 17577-28-5

PROPERTIES

Melting Point 120-123 °C(lit.)
Melting Point 120-123 °C (dec.)
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 dust mask type N95 (US), Eyeshields, Gloves
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
Storage Temperature 2-8°C
German water hazard class 3
Grade technical
Linear Formula CH3CH2OCOCH2P(Cl)(C6H5)3
Purity ≥90% (AT)

DETAILS

Description (English)
Other Notes
Starting material for preparing the Wittig-reagent6,7,8
Application
Reactant for:
• Preparation of disubstituted tetrahydrofurans as selective serotonin re-uptake inhibitors for the treatment of depression1
• Ring-opening reactions with Wittig reagents2
• Enantioselective total synthesis of the phytotoxic lactone herbarumin III via Keck′s asymmetric allylation and Sharpless epoxidation3
• Synthesis of fluorobenzofurans via microwave-assisted tandem intramolecular Wittig and Claisen rearrangement reactions4
• Preparation of phosphonium derivatives of coumarin5
Description (简体中文)
Other Notes
制备 Wittig 试剂的原料6,7,8
Application
Reactant for:
• Preparation of disubstituted tetrahydrofurans as selective serotonin re-uptake inhibitors for the treatment of depression1
• Ring-opening reactions with Wittig reagents2
• Enantioselective total synthesis of the phytotoxic lactone herbarumin III via Keck′s asymmetric allylation and Sharpless epoxidation3
• Synthesis of fluorobenzofurans via microwave-assisted tandem intramolecular Wittig and Claisen rearrangement reactions4
• Preparation of phosphonium derivatives of coumarin5

REFERENCES