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2-(Trimethylsilyl)ethoxymethyl-triphenylphosphonium chloride_Molecular_structure_CAS_82495-75-8)
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2-(Trimethylsilyl)ethoxymethyl-triphenylphosphonium chloride

Catalog No. 330671 Name Sigma Aldrich
CAS Number 82495-75-8 Website http://www.sigmaaldrich.com
M. F. C24H30ClOPSi Telephone 1-800-521-8956
M. W. 429.006661 Fax
Purity 98% Email
Storage Chembase ID: 147680

SYNONYMS

Title
2-(三甲基硅烷)乙氧三苯甲基氯化膦
IUPAC name
triphenyl({[2-(trimethylsilyl)ethoxy]methyl})phosphanium chloride
IUPAC Traditional name
triphenyl({[2-(trimethylsilyl)ethoxy]methyl})phosphanium chloride
Synonyms
SEM-三苯基氯化磷
SEM-triphenylphosphonium chloride

DATABASE IDS

Beilstein Number 4632507
CAS Number 82495-75-8
PubChem SID 24859880
MDL Number MFCD00043159

PROPERTIES

Linear Formula (CH3)3SiCH2CH2OCH2P(C6H5)3Cl
Purity 98%
Melting Point 145-149 °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 dust mask type N95 (US), Eyeshields, Gloves
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
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective synthesis of (-)-sarain A using asymmetric Michael addition, cyclization, ring-closing metathesis, intramolecular Stille coupling, and late-state installation of tertiary amine-aldehyde proximity interaction1
• Preparation of aliphatic and alicyclic aldehydes by homologation of aldehydes2
• Wittig reactions3
• Preparation of optically active (1S,5R)-(+)-3-azabicyclo[3.2.2]non-6-en-2-one via enantioselective intramolecular cyclopropanation4
Description (简体中文)
包装
1, 5 g in glass bottle
Application
Reactant for:
• Enantioselective synthesis of (-)-sarain A using asymmetric Michael addition, cyclization, ring-closing metathesis, intramolecular Stille coupling, and late-state installation of tertiary amine-aldehyde proximity interaction1
• Preparation of aliphatic and alicyclic aldehydes by homologation of aldehydes2
• Wittig reactions3
• Preparation of optically active (1S,5R)-(+)-3-azabicyclo[3.2.2]non-6-en-2-one via enantioselective intramolecular cyclopropanation4

REFERENCES