Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C12H10N3O3P |
| Molecular Weight | 275.1999 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
[N-]=[N+]=NP(=O)(OC1=CC=CC=C1)OC2=CC=CC=C2
InChI
InChIKey=SORGEQQSQGNZFI-UHFFFAOYSA-N
InChI=1S/C12H10N3O3P/c13-14-15-19(16,17-11-7-3-1-4-8-11)18-12-9-5-2-6-10-12/h1-10H
| Molecular Formula | C12H10N3O3P |
| Molecular Weight | 275.1999 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 1 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Gelatinases in soft tissue biomaterials. Analysis of different crosslinking agents. | 2002 Aug |
|
| Cobalt-catalyzed asymmetric olefin aziridination with diphenylphosphoryl azide. | 2008 Sep 19 |
|
| Ultrafast spectroscopy and computational study of the photochemistry of diphenylphosphoryl azide: direct spectroscopic observation of a singlet phosphorylnitrene. | 2010 Dec 1 |
|
| Ultrasound-targeted microbubble destruction mediated herpes simplex virus-thymidine kinase gene treats hepatoma in mice. | 2010 Dec 23 |
|
| Thiazole and oxazole alkaloids: isolation and synthesis. | 2010 Nov 5 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 04:17:31 GMT 2023
by
admin
on
Sat Dec 16 04:17:31 GMT 2023
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| Record UNII |
GXM91165AV
|
| Record Status |
Validated (UNII)
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| Record Version |
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GXM91165AV
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26386-88-9
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DIPHENYLPHOSPHORYL AZIDE
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123414
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247-644-0
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m4636
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DTXSID10949274
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