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Diethyl (1-cyanoethyl)phosphonate_Molecular_structure_CAS_29668-61-9)
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Diethyl (1-cyanoethyl)phosphonate

Catalog No. 408573 Name Sigma Aldrich
CAS Number 29668-61-9 Website http://www.sigmaaldrich.com
M. F. C7H14NO3P Telephone 1-800-521-8956
M. W. 191.164721 Fax
Purity 97% Email
Storage Chembase ID: 145281

SYNONYMS

Title
二乙基(1-氰乙基)膦酸酯
IUPAC name
diethyl (1-cyanoethyl)phosphonate
IUPAC Traditional name
diethyl 1-cyanoethylphosphonate
Synonyms
NSC 135193
(1-Cyanoethyl)phosphonic acid diethyl ester

DATABASE IDS

PubChem SID 24865577
MDL Number MFCD01457302
CAS Number 29668-61-9

PROPERTIES

Linear Formula CH3CH(CN)P(O)(OC2H5)2
Purity 97%
Boiling Point 140-141 °C/11 mmHg(lit.)
Density 1.085 g/mL at 25 °C(lit.)
Flash Point 113 °C
Flash Point 235.4 °F
Refractive Index n20/D 1.432(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 (简体中文)
包装
5 g in glass bottle
Application
Reacant for:
• Preparation of sphingosine phosphate receptor (S1P) agonists with N-cinnamyl-β-alanine moiety1
• Preparation of benzyl- and benzoyldimethylaminopyridinones as HIV-1 reverse transcriptase inhibitors2
• Stereoselective preparation of cyano(trifluoromethyl)pentenenitriles via alkylation, followed by elimination reaction3
• Synthesis of [(methylenepiperidinyl) or (methylenepyrrolidinyl)fluorophenyl]oxazolidinone antibacterial agents4
• Horner-Wadsworth-Emmons olefination5
Description (English)
Packaging
5 g in glass bottle
Application
Reacant for:
• Preparation of sphingosine phosphate receptor (S1P) agonists with N-cinnamyl-β-alanine moiety1
• Preparation of benzyl- and benzoyldimethylaminopyridinones as HIV-1 reverse transcriptase inhibitors2
• Stereoselective preparation of cyano(trifluoromethyl)pentenenitriles via alkylation, followed by elimination reaction3
• Synthesis of [(methylenepiperidinyl) or (methylenepyrrolidinyl)fluorophenyl]oxazolidinone antibacterial agents4
• Horner-Wadsworth-Emmons olefination5

REFERENCES