Diphenylazidophosphat

Diphenylphosphoryl azide Struktur
26386-88-9
CAS-Nr.
26386-88-9
Bezeichnung:
Diphenylazidophosphat
Englisch Name:
Diphenylphosphoryl azide
Synonyma:
DPPA;DIPHENYL PHOSPHORAZIDATE;DIPHENYLPHOSPHONIC AZIDE;DIPHENYL AZIDOPHOSPHATE;diphenylphophoryl azide;Diphenylphosphorazindate(DPPA);Diphenyphosphoryl azide;Diphenyl azide phosphate;phosphorazidicacid,diphenylester;PS-DPPA
CBNumber:
CB3404964
Summenformel:
C12H10N3O3P
Molgewicht:
275.2
MOL-Datei:
26386-88-9.mol

Diphenylazidophosphat Eigenschaften

Siedepunkt:
157 °C/0.17 mmHg (lit.)
Dichte
1.277 g/mL at 25 °C (lit.)
Brechungsindex
n20/D 1.551(lit.)
Flammpunkt:
>230 °F
storage temp. 
2-8°C
Löslichkeit
Acetonitrile (Slightly), Chloroform (Slightly), Ethyl Acetate (Sparingly)
Aggregatzustand
Liquid
Wichte
1.277
Farbe
slightly yellow
Wasserlöslichkeit
insoluble
Hydrolytic Sensitivity
7: reacts slowly with moisture/water
BRN 
2058967
Stabilität:
Stable. Incompatible with acids, strong oxidizing agents.
InChIKey
SORGEQQSQGNZFI-UHFFFAOYSA-N
CAS Datenbank
26386-88-9(CAS DataBase Reference)
NIST chemische Informationen
Diphenylphosphoryl azide(26386-88-9)
Sicherheit
  • Risiko- und Sicherheitserklärung
  • Gefahreninformationscode (GHS)
Kennzeichnung gefährlicher T
R-Sätze: 23/24/25-36/37/38
S-Sätze: 26-36/37/39-45
RIDADR  UN 3278 6.1/PG 2
WGK Germany  3
3-10
Hazard Note  Toxic/Keep Cold
TSCA  No
HazardClass  6.1
PackingGroup  III
HS Code  29299000
Bildanzeige (GHS) GHS hazard pictograms
Alarmwort Achtung
Gefahrenhinweise
Code Gefahrenhinweise Gefahrenklasse Abteilung Alarmwort Symbol P-Code
H315 Verursacht Hautreizungen. Hautreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P302+P352, P321,P332+P313, P362
H319 Verursacht schwere Augenreizung. Schwere Augenreizung Kategorie 2 Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" /> P264, P280, P305+P351+P338,P337+P313P
H335 Kann die Atemwege reizen. Spezifische Zielorgan-Toxizität (einmalige Exposition) Kategorie 3 (Atemwegsreizung) Warnung GHS hazard pictogramssrc="/GHS07.jpg" width="20" height="20" />
Sicherheit
P261 Einatmen von Staub vermeiden.
P280 Schutzhandschuhe/Schutzkleidung/Augenschutz tragen.
P301+P310 BEI VERSCHLUCKEN: Sofort GIFTINFORMATIONSZENTRUM/Arzt/... (geeignete Stelle für medizinische Notfallversorgung vom Hersteller/Lieferanten anzugeben) anrufen.
P305+P351+P338 BEI KONTAKT MIT DEN AUGEN: Einige Minuten lang behutsam mit Wasser spülen. Eventuell vorhandene Kontaktlinsen nach Möglichkeit entfernen. Weiter spülen.

Diphenylazidophosphat Chemische Eigenschaften,Einsatz,Produktion Methoden

R-Sätze Betriebsanweisung:

R23/24/25:Giftig beim Einatmen, Verschlucken und Berührung mit der Haut.
R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut.

S-Sätze Betriebsanweisung:

S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren.
S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen.
S45:Bei Unfall oder Unwohlsein sofort Arzt zuziehen (wenn möglich, dieses Etikett vorzeigen).

Chemische Eigenschaften

Diphenylphosphoryl azide (DPPA) is a colorless or pale yellow liquid which boils at 134-136 °C/0.2 mmHg, and it will be stable at room temperature under shading. It is non-explosive just like the other phosphorazidate. When DPPA is stored at room temperature for a long time, it might be slowly and partially hydrolyzed with moisture in air to produce diphenyl phosphate and toxic explosive hydrazoic acid. In this case, it will be recommended to use after washing DPPA with aqueous sodium hydrogen carbonate followed by drying.

Verwenden

Diphenylphosphoryl azide (DPPA or diphenyl phosphorazidate, (PhO)2P(O)N3) is a very toxic and potentially explosive organic compound. DPPA has been found to be effective for a variety of organic reactions as a versatile synthetic reagent. It is widely used in synthesis of other organic compounds especially as a reagent for the synthesis of peptides by virtue of its reactions with carboxylic acids leading to either the urethane or the amide.

synthetische

Diphenylphosphoryl azide (DPPA) is easily prepared in high yield by the reaction of the corresponding chloride with sodium azide in acetone. Combination of sodium azide and 18-crown-6 in the same reaction was reported, and the use of a quaternary ammonium salt as a phase-transfer catalyst in a biphasic phase of water and an organic solvent was also reported to be effective, as shown in Scheme 3.
synthesis of Diphenyl Phosphorazidate (DPPA)
Diphenyl Phosphorazidate (DPPA) - More Than Three Decades Later
Takayuki Shioiri
Graduate School of Environmental and Human Sciences, Meijo University

Application

Diphenylphosphoryl azide (DPPA) is a well-known azide reagent used in peptide couplings, Curtius rearrangements, and Mitsunobu inversions—is often encountered in pharmaceutical process development because it enables the most direct route to a desired product. Diphenylphosphonic azide acts as a reagent for the synthesis of peptides and phosphoramidates by reacting with amines. It is also used in the preparation of oligosaccharides linked with carbamate and urea bonds utilizing modified Curtis rearrangement. It is involved in pseudohalogen replacement of the azido group by treatment with nucleophilic reagents, such as water, butanol, ammonia, and various amines. Further, it is used as a hydroazidation catalyst for preparation of organoazides.

Reaktionen

Diphenylphosphoryl azide, originally developed by Yamada in 1972, has shown significant synthetic versatility, being used in isocyanate synthesis, especially in the Curtius rearrangement, stereospecific conversion of alcohol into azide, as a coupling reagent in macrolactamization[4], in allylic amine synthesis, and in aziridination reactions. Diphenylphosphoryl azide, also called DPPA, diphenyl phosphorazidate or phosphoric acid diphenyl ester azide, is a colorless liquid with high boiling point (157 ??C/0.17 mmHg), and can be easily prepared by the reaction between diphenylphosphoryl chloride and sodium azide in acetone in high yield. The Waldvogel group developed a reliable protocol for the large-scale (100 g) synthesis of DPPA, including purification by reduced-pressure distillation (Picture 1). A polymer-supported form of the reagent has also been developed using phenol resin by the Taylor group.
Reactions of 26386-88-9

Mechanism of action

Diphenyl phosphoryl azide is used in the aziridination of olefins catalyzed by colbalt-tetraphenylporphyrin. It is also used as the activating agent in the preparation of macrocyclic lactams and of an aldose reductase inhibitor.

Diphenylazidophosphat Upstream-Materialien And Downstream Produkte

Upstream-Materialien

Downstream Produkte


Diphenylazidophosphat Anbieter Lieferant Produzent Hersteller Vertrieb Händler.

Global( 570)Lieferanten
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Nanjing Sinoda Biological Technology Co., Ltd
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26386-88-9(Diphenylazidophosphat)Verwandte Suche:


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  • PHOSPHORIC ACID DIPHENYL ESTER AZIDE
  • PS-DPPA
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  • DPPA polymer-bound, PS-DPPA
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  • DIPHENYLPHOSPHORYL AZIDE
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  • DPPA, Diphenyl phosphorazidate, Diphenyl azidophosphonate
  • Diphenylphosphoryl Azide (DPPA)
  • Diphenyl phosphonyl azide
  • Phosphorazidic acid, diphenyl ester
  • Diphenylphoshoryl azide
  • DIPHENYL AZIDOPHOSPHATE FOR SYNTHESIS
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  • DIPHENYL PHOSPHORAZIDATE
  • DIPHENYL AZIDOPHOSPHATE
  • diphenylphophoryl azide
  • Diphenyphosphoryl azide
  • Relebactam Impurity 3
  • Diphenyl Phophoryl Azide(DPPA)
  • 26386-88-9
  • 26286-88-9
  • 26386-88-6
  • C12H10N3O3P
  • C12H10O3N3P
  • C6H5O2PON3
  • Peptide Synthesis
  • Amination
  • Condensation & Active Esterification
  • Coupling Reactions (Peptide Synthesis)
  • C-X Bond Formation (Non-Halogen)
  • Synthetic Reagents
  • Azidation/Diazo Transfer
  • Pharmaceutical Intermediates
  • Peptide Coupling Reagents
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