37097-43-1

Basic information

• Product Name: DIETHOXYMORPHOLINOPHOSPHINEOXIDE
• Synonyms: DIETHOXYMORPHOLINOPHOSPHINEOXIDE;Morpholinophosphonic acid diethyl;Morpholinophosphonic acid diethyl ester
• CAS NO: 37097-43-1
• Molecular Formula: C₈H₁₈NO₄P
• Molecular Weight: 223.2066
• Mol File: 37097-43-1.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 282.7°Cat760mmHg
• Flash Point: 124.8°C
• Appearance: /
• Density: 1.15g/cm³
• Vapor Pressure: 0.0033mmHg at 25°C
• Refractive Index: 1.457
• CAS DataBase Reference: DIETHOXYMORPHOLINOPHOSPHINEOXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHOXYMORPHOLINOPHOSPHINEOXIDE(37097-43-1)
• EPA Substance Registry System: DIETHOXYMORPHOLINOPHOSPHINEOXIDE(37097-43-1)

Safety Data

• Hazardous Substances Data: 37097-43-1(Hazardous Substances Data)

Usage

InChI:InChI=1/C8H18NO4P/c1-3-12-14(10,13-4-2)9-5-7-11-8-6-9/h3-8H2,1-2H3

Upstream product

• 74178-27-1 di-p-chlorophenyl morpholidophosphate 
• 64-17-5 ethanol 
• 7412-25-1 morpholinodiphenylphosphine oxide 
• 110-91-8 morpholine 
• 762-04-9 phosphonic acid diethyl ester 
• 311-45-5 paraoxon 
• 102-77-2 4-(benzothiazole-2-sulfenyl)-morpholine 
• 122-52-1 triethyl phosphite 
• 762-04-9 Diethyl phosphonate 
• 74178-28-2 di-m-nitrophenyl morpholidophosphate 
• 74178-25-9 di-p-methoxyphenyl morpholidophosphate 
• 74178-26-0 di-p-methylphenyl morpholidophosphate 
• 4837-31-4 4-Phenylsulfanyl-morpholine 
• 2958-89-6 N-(chlorosulfanyl)morpholine 

Relevant articles and documents

Phosphoramidate synthesis via copper-catalysed aerobic oxidative coupling of amines and H-phosphonates

The copper-catalysed oxidative coupling of amines and H-phosphonates to produce phosphoramidates has been achieved using CuI as the catalyst and O 2 (present in air) as the sole oxidant.

REACTIONS OF 4-MORPHOLINESULFENYL CHLORIDE WITH TRIALKYL PHOSPHITES

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REACTION OF SULFENAMIDES WITH DI-ALKYL AND TRIALKYL PHOSPHITES. AN EFFICIENT SYNTHESIS OF PHOSPHORAMIDATES BY UNUSUAL SUBSTITUTION AT S-N BOND IN (2-BENZOTHIAZOLYL)SULFENAMIDES

Regioselective attack of the trivalent phosphorus atom of dialkyl and trialkyl phosphites on either nitrogen or sulfur atom of sulfenamides has been found.The reaction of phenylsulfenamides with dialkyl phosphites yielded phosphorothiolates, whereas the treatment of (2-benzothiazolyl)sulfenamides with dialkyl and trialkyl phosphites gave phosphoramidates in excellent yields.