Details
Stereochemistry | ACHIRAL |
Molecular Formula | C5H4N4O |
Molecular Weight | 136.1115 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
ON1N=NC2=CC=CN=C12
InChI
InChIKey=FPIRBHDGWMWJEP-UHFFFAOYSA-N
InChI=1S/C5H4N4O/c10-9-5-4(7-8-9)2-1-3-6-5/h1-3,10H
Approval Year
PubMed
Title | Date | PubMed |
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Introduction to peptide synthesis. | 2002 Aug |
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Organophosphorus and nitro-substituted sulfonate esters of 1-hydroxy-7-azabenzotriazole as highly efficient fast-acting peptide coupling reagents. | 2004 Jan 9 |
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DNA display III. Solid-phase organic synthesis on unprotected DNA. | 2004 Jul |
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Total synthesis of cyclosporin O: exploring the utility of Bsmoc-NMe-amino acid fluorides and KOAt. | 2009 |
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Synthesis and application of N-[1-(4-(4-fluorophenyl)-2,6-dioxocyclohexylidene)ethyl] (Fde)-protected amino acids for optimization of solid-phase peptide synthesis using gel-phase (19)F NMR spectroscopy. | 2009 Apr |
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Monoporphyrinate ytterbium(iii) complexes with new ancillary ligands: synthesis, structural analysis and photophysical investigation. | 2009 Jun 28 |
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Reactions of monoaryl-substituted methylenecyclobutanes and methylenecyclopropanes with 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), and 1-hydroxysuccinimide (HOSu). | 2009 Mar 20 |
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Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. | 2009 Sep 21 |
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Sulfonate esters of 1-hydroxypyridin-2(1H)-one and ethyl 2-cyano-2-(hydroxyimino)acetate (oxyma) as effective peptide coupling reagents to replace 1-hydroxybenzotriazole and 1-hydroxy-7-azabenzotriazole. | 2010 Apr |
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Reactivity and applications of new amine reactive cross-linkers for mass spectrometric detection of protein-protein complexes. | 2010 Jan 1 |
Patents
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Code System | Code | Type | Description | ||
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181649
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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PRIMARY | |||
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1-HYDROXY-7-AZABENZOTRIAZOLE
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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DTXSID0075239
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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39968-33-7
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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C435757
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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TX8XYH09H0
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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m6118
Created by
admin on Sat Dec 16 02:03:19 GMT 2023 , Edited by admin on Sat Dec 16 02:03:19 GMT 2023
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PRIMARY | Merck Index |
SUBSTANCE RECORD