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Structure

Diethyl cyanidophosphate

CAS
2942-58-7
Catalog Number
ACM2942587
Category
Other Products
Molecular Weight
163.11
Molecular Formula
C5H10NO3P

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Specification

Synonyms
Diethylcyanophosphate, Diethyl cyanophosphonate, Diethyl cyanidophosphate, Diethylphosphorocyanidate, DEPC, Diethyl phosphorocyanidate, Diethoxy-phosphoryl cyanide, Diethyl cyanophosphosphonate, Diethyl phosphoryl cyanide, Phosphorocyanidic acid, diethyl ester, 472565_ALDRICH, EINECS 220-936-5, BRN 1768938, Phosphorocyanidic acid, O,O-diethyl ester, LS-107948, 4-03-00-00265 (Beilstein Handbook Reference), 2942-58-7
IUPAC Name
diethoxyphosphorylformonitrile
Canonical SMILES
CCOP(=O)(C#N)OCC
InChI Key
ZWWWLCMDTZFSOO-UHFFFAOYSA-N
Boiling Point
104-105ºC (19 mmHg)
Flash Point
80ºC
Density
1.075
Appearance
UN 2922 8/PG 2
EC Number
220-936-5
Exact Mass
163.04000
Hazard Statements
T+:Verytoxic;C:Corrosive;
H-Bond Acceptor
4
H-Bond Donor
0
Packing Group
II
Safety Description
S26-S28-S36/37/39-S45-S50
Stability
Stable under normal temperatures and pressures.
WGK Germany
3

Downstream Synthesis Route 1

  • 29943-42-8
  • 2942-58-7
  • 4295-99-2

Reference: [1] Patent: US6372778, 2002, B1, . Location in patent: Example 80

Downstream Synthesis Route 2

  • 3612-20-2
  • 2942-58-7
  • 62718-31-4

Reference: [1] Organic Process Research and Development, 2012, vol. 16, # 12, p. 1927 - 1939

Downstream Synthesis Route 3

  • 2942-58-7
  • 2338-75-2

Reference: [1] Chemistry Letters, 2004, vol. 33, # 9, p. 1192 - 1193
[2] Bulletin of the Chemical Society of Japan, 2006, vol. 79, # 7, p. 1106 - 1117

Downstream Synthesis Route 4

  • 2942-58-7
  • 19741-14-1
  • 6234-01-1
  • 79640-68-9
  • 95485-10-2
  • 95485-11-3

Reference: [1]Heterocycles,1981,vol. 15,p. 981 - 984
[2]Patent: WO2011/79114,2011,A1 .Location in patent: Page/Page column 108; 109

Downstream Synthesis Route 5

  • 2942-58-7
  • 529-34-0
  • 132205-64-2

Reference: [1]Journal of Medicinal Chemistry,1985,vol. 28,p. 660 - 667

Downstream Synthesis Route 6

  • 2942-58-7
  • 2999-46-4
  • 25016-20-0
  • 1026454-77-2

Reference: [1]Journal of the Chemical Society. Perkin transactions I,1990,p. 607 - 610

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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