Jump to content

DEPBT

From Wikipedia, the free encyclopedia

This is an old revision of this page, as edited by Mfernflower (talk | contribs) at 01:43, 19 June 2018 (added Category:Organophosphates using HotCat). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

DEPBT
Names
IUPAC name
3-(Diethoxyphosphoryloxy)-1,2,3- benzotriazin-4(3H)-one
Other names
DEPBT
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.156.337 Edit this at Wikidata
  • InChI=1S/C11H14N3O5P/c1-3-17-20(16,18-4-2)19-14-11(15)9-7-5-6-8-10(9)12-13-14/h5-8H,3-4H2,1-2H3
    Key: AJDPNPAGZMZOMN-UHFFFAOYSA-N
  • CCOP(=O)(OCC)On1c(=O)c2ccccc2nn1
Properties
C11H14N3O5P
Molar mass 299.22 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N (what is checkY☒N ?)


DEPBT (3-(diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one) is a peptide coupling reagent used in peptide synthesis. It shows remarkable resistance to racemization.[1]

See also

References

  1. ^ Li, Haitao; Jiang, Xiaohui; Ye, Yun-hua; Fan, Chongxu; Romoff, Todd; Goodman, Murray (1999). "3-(Diethoxyphosphoryloxy)-1,2,3- benzotriazin-4(3H)-one (DEPBT): A New Coupling Reagent with Remarkable Resistance to Racemization". Organic Letters. 1 (1): 91–94. doi:10.1021/ol990573k. ISSN 1523-7060.