1946-09-4

Basic information

• Product Name: diethyl ethylphosphoramidate
• CAS NO: 1946-09-4
• Molecular Formula: C₆H₁₆NO₃P
• Molecular Weight: 181.1699
• Mol File: 1946-09-4.mol

Chemical Properties

• Boiling Point: 204.2°C at 760 mmHg
• Flash Point: 77.3°C
• Density: 1.045g/cm³
• Vapor Pressure: 0.266mmHg at 25°C
• Refractive Index: 1.419
• CAS DataBase Reference: diethyl ethylphosphoramidate(CAS DataBase Reference)
• NIST Chemistry Reference: diethyl ethylphosphoramidate(1946-09-4)
• EPA Substance Registry System: diethyl ethylphosphoramidate(1946-09-4)

Safety Data

• Hazardous Substances Data: 1946-09-4(Hazardous Substances Data)

Upstream product

• 61056-26-6 ethylphosphoramidic acid dichloride 
• 141-52-6 sodium ethanolate 
• 557-66-4 ethanamine hydrochloride 
• 762-04-9 phosphonic acid diethyl ester 
• 74-96-4 ethyl bromide 
• 40923-48-6 diethyl N-(trimethylsilyl)phosphoroamidate 
• 85231-90-9 C₁₁H₂₄NO₅P 
• 122-52-1 triethyl phosphite 
• 75-04-7 ethylamine 
• 814-49-3 diethyl chlorophosphate 

Downstream Products

• 13360-63-9 N-ethylbutylamine 
• 624-78-2 N-Ethylmethylamine 
• 20193-20-8 ethylpropylamine 
• 2424-02-4 allylethylamine 
• 914941-63-2 diethoxy[N-(4-oxo-4-phenoxy-Δ²1,3,4-oxazaphospholin-2-yl)-N-ethyl]amidophosphate 
• 91691-46-2 Phosphorsaeure-diaethylester- 
• 53897-00-0 C₅H₅Fe(CO)(CNC₂H₅)P(C₆H₅)3⁽¹⁺⁾*PF₆^(1-)=C₅H₅Fe(CO)(CNC₂H₅)P(C₆H₅)3PF₆ 

Relevant articles and documents

One-step transformation of ammonium dialkyl phosphoroselenoates into dialkyl phosphoramidates

Ammonium dialkyl phosphoroselenoates are directly converted into the dialkyl phosphoramidates by iodosobenzene and iodoxybenzene. The inversion of configuration at the phosphorus atom, using model diastereoisomeric ammonium cis- and trans-2-oxo-2-seleno-4-methyl-1,3,2-dioxaphosphinan system, was observed. The mechanistic scheme of this transformation is discussed.

Phosphoramidate-mediated conversion of carbonyl ligands into isocyanide ligands: A new approach to chiral isocyanide ligands

Metal isocyanides have been used and studied by organometallic chemists for many years and, as a result, they have a rich and interesting chemistry. The nature of metal-free isocyanides and the methods of making isocyanide complexes, however, has resulted

Phosphoramidate-mediated conversion of metal carbonyls into metal isonitriles

The reaction of metal carbonyls with readily-available phosphoramidate anions provides a new route to metal isonitriles; in particular, enantiomerically pure isonitrile complexes are easily accessed by this method.

Fungicides for the control of take-all disease of plants

A method of controlling Take-All disease of plants by applying a fungicide of the formula STR1 wherein Z1 and Z2 are C and are part of an aromatic ring which is benzothiophene; and A is selected from --C(X)-amine wherein the amine is an unsubstituted, monosubstituted or disubstituted amino radical, --C(O)--SR3, --NH--C(X)R4, and --C(=NR3)--XR7 ; B is --Wm --Q(R2)3 or selected from O-tolyl, 1-naphthyl, 2-naphthyl, and 9-phenanthryl, each optionally substituted with halogen or R4 ; Q is C, Si, Ge, or Sn; W is --C(R3)p H(2-p) --; or when Q is C, W is selected from --C(R3)p H(2-p), --N(R3)m H(1-m)--, --S(O)p--, and --O--; X is 0 or S; n is 0, 1, 2, or 3; m is 0 or 1; p is 0, 1, or 2; each R and R2 is independently defined herein; R3 is C1 -C4 alkyl; R4 is C1 -C4 alkyl, haloalkyl, alkoxy, alkylthio, alkylamino, or dialkylamino; and R7 is C1 -C4 alkyl, haloalkyl, or phenyl, optionally substituted with halo, nitro, or R4 ; or an agronomic salt thereof.