COMU

from Wikipedia, the free encyclopedia
Structural formula
HCTU and analogues
General
Surname COMU
other names

(1-Cyano-2-ethoxy-2-oxoethylideneaminooxy) dimethylamino-morpholino-carbenium-hexafluorophosphate

Molecular formula C 12 H 19 F 6 N 4 O 4 P
External identifiers / databases
CAS number 1075198-30-9
EC number 682-899-5
ECHA InfoCard 100.208.431
PubChem 44471148
ChemSpider 26496276
Wikidata Q20650188
properties
Molar mass 428.27 g mol −1
Physical state

firmly

safety instructions
GHS labeling of hazardous substances
no GHS pictograms
H and P phrases H: no H-phrases
P: no P-phrases
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions .

COMU [(1-cyano-2-ethoxy-2-oxoethylideneaminooxy) dimethylamino-morpholino-carbenium-hexafluorophosphate] is a coupling reagent which is used in peptide synthesis to generate peptides .

Alternative coupling reagents are e.g. B. HATU , HBTU , HCTU , TBTU , TOMBU and COMBU .

Individual evidence

  1. a b COMU® data sheet at Sigma-Aldrich , accessed on October 18, 2016 ( PDF ).
  2. R. Subirós-Funosas, L. Nieto-Rodriguez, KJ Jensen, F. Albericio: COMU: scope and limitations of the latest innovation in peptide acyl transfer reagents. In: Journal of Peptide Science . Volume 19, Number 7, July 2013, pp. 408-414, doi : 10.1002 / psc.2517 , PMID 23712932 .
  3. CU Hjørringgaard, A. Brust, PF Alewood: Evaluation of COMU as a coupling reagent for in situ neutralization Boc solid phase peptide synthesis. In: Journal of Peptide Science. Volume 18, Number 3, March 2012, pp. 199-207, doi : 10.1002 / psc.1438 , PMID 22252935 .
  4. YE Jad, SN Khattab, BG de la Torre, T. Govender, HG Kruger, A. El-Faham, F. Albericio: TOMBU and COMBU as Novel Uronium-type peptide coupling reagents derived from Oxyma-B. In: Molecules. Volume 19, number 11, 2014, pp. 18953-18965, doi : 10.3390 / molecules191118953 , PMID 25412042 .