Diethyl (2-cyanoethyl)phosphonate

• Catalog No.: 551163
• CAS Number: 10123-62-3
• M. F.: C7H14NO3P
• M. W.: 191.164721
• Purity: 95%

SYNONYMS

• Title: 二乙基(2-氰乙基)膦酸酯
• IUPAC name: diethyl (2-cyanoethyl)phosphonate
• IUPAC Traditional name: diethyl 2-cyanoethylphosphonate
• Synonyms: (2-Cyanoethyl)-phosphonic acid diethyl ester; (2-氰乙基)-膦酸二乙酯; NSC 43781; NSC 74863; 3-(Diethylphosphono)propionitrile

DATABASE IDS

• PubChem SID: 24879203
• CAS Number: 10123-62-3
• MDL Number: MFCD00013825
• EC Number: 233-327-4

PROPERTIES

• Linear Formula: NC(CH2)2P(O)(OC2H5)2
• Purity: 95%
• Boiling Point: 110 °C/0.1 mmHg(lit.)
• Density: 1.08 g/mL at 25 °C(lit.)
• Refractive Index: n20/D 1.4380(lit.)
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• 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
• RTECS: KI6650000
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant for:
• Heteroatom-directed alkyl cyanation of alkynes1
• Use as a fluorescent substrate for carbon-phosphorous lyase2
• Microwave-assisted cleavage of phosphate, phosphonate, and phorphoramide esters3
• Amination and stereoselective olefination for synthesis of HIV-1 antivirals4Reactant for synthesis of:
• Base-catalyzed stereospecific anti-Markovnikov addition reactants5
• Lipophilic oxoamides with activity against phospholipase A26
• Triose phosphate isomerase of muscle inhibitors7

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant for:
• Heteroatom-directed alkyl cyanation of alkynes1
• Use as a fluorescent substrate for carbon-phosphorous lyase2
• Microwave-assisted cleavage of phosphate, phosphonate, and phorphoramide esters3
• Amination and stereoselective olefination for synthesis of HIV-1 antivirals4Reactant for synthesis of:
• Base-catalyzed stereospecific anti-Markovnikov addition reactants5
• Lipophilic oxoamides with activity against phospholipase A26
• Triose phosphate isomerase of muscle inhibitors7