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HOAT 1M DMA solution

CAS No.:
39968-33-7
Catalog Number:
AG0032SC
Molecular Formula:
C5H4N4O
Molecular Weight:
136.1115
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
5g
98%
In Stock USA
United States
$32
- +
25g
98%
In Stock USA
United States
$100
- +
100g
98%
In Stock USA
United States
$300
- +
Product Description
Catalog Number:
AG0032SC
Chemical Name:
HOAT 1M DMA solution
CAS Number:
39968-33-7
Molecular Formula:
C5H4N4O
Molecular Weight:
136.1115
MDL Number:
MFCD00210053
IUPAC Name:
3-hydroxytriazolo[4,5-b]pyridine
InChI:
InChI=1S/C5H4N4O/c10-9-5-4(7-8-9)2-1-3-6-5/h1-3,10H
InChI Key:
FPIRBHDGWMWJEP-UHFFFAOYSA-N
SMILES:
On1nnc2c1nccc2
UNII:
TX8XYH09H0
Properties
Complexity:
131  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
136.039g/mol
Formal Charge:
0
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0
Molecular Weight:
136.114g/mol
Monoisotopic Mass:
136.039g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
63.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.5  
Literature
Title Journal
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Chemical synthesis and biological activity of analogues of the lantibiotic epilancin 15X. Journal of the American Chemical Society 20120509
Synthesis of 5'-terminal capped oligonucleotides using O-N phosphoryl migration of phosphoramidite derivatives. Organic letters 20120106
Triostin A derived hybrid for simultaneous DNA binding and metal coordination. Amino acids 20110701
Piperazines for peptide carboxyl group derivatization: effect of derivatization reagents and properties of peptides on signal enhancement in matrix-assisted laser desorption/ionization mass spectrometry. Rapid communications in mass spectrometry : RCM 20110315
Design of glycopeptides used to investigate class II MHC binding and T-cell responses associated with autoimmune arthritis. PloS one 20110101
Ultraviolet photodissociation of carboxylate-derivatized peptides in a quadrupole ion trap. Journal of the American Society for Mass Spectrometry 20110101
Mastering the canonical loop of serine protease inhibitors: enhancing potency by optimising the internal hydrogen bond network. PloS one 20110101
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. Chemical & pharmaceutical bulletin 20100401
Reactivity and applications of new amine reactive cross-linkers for mass spectrometric detection of protein-protein complexes. Analytical chemistry 20100101
Oxyma: an efficient additive for peptide synthesis to replace the benzotriazole-based HOBt and HOAt with a lower risk of explosion. Chemistry (Weinheim an der Bergstrasse, Germany) 20090921
COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents. Chemistry (Weinheim an der Bergstrasse, Germany) 20090921
Monoporphyrinate ytterbium(iii) complexes with new ancillary ligands: synthesis, structural analysis and photophysical investigation. Dalton transactions (Cambridge, England : 2003) 20090628
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. Journal of peptide science : an official publication of the European Peptide Society 20090401
Reactions of monoaryl-substituted methylenecyclobutanes and methylenecyclopropanes with 1-hydroxybenzotriazole (HOBt), 1-hydroxy-7-azabenzotriazole (HOAt), and 1-hydroxysuccinimide (HOSu). The Journal of organic chemistry 20090320
Total synthesis of cyclosporin O: exploring the utility of Bsmoc-NMe-amino acid fluorides and KOAt. Protein and peptide letters 20090101
Nucleophilic carbene and HOAt relay catalysis in an amide bond coupling: an orthogonal peptide bond forming reaction. Journal of the American Chemical Society 20071114
Blind crystal structure prediction of a novel second polymorph of 1-hydroxy-7-azabenzotriazole. Acta crystallographica. Section B, Structural science 20060801
Catalytic ester-amide exchange using group (IV) metal alkoxide-activator complexes. Journal of the American Chemical Society 20050720
Three-dimensional arrangement of sugar residues along helical polypeptide backbone. 2. Synthesis of periodic N-glycosylated peptides by polymerization of tripeptide active esters containing alpha,alpha-disubstituted amino acid. Biomacromolecules 20050101
DNA display III. Solid-phase organic synthesis on unprotected DNA. PLoS biology 20040701
Organophosphorus and nitro-substituted sulfonate esters of 1-hydroxy-7-azabenzotriazole as highly efficient fast-acting peptide coupling reagents. The Journal of organic chemistry 20040109
Introduction to peptide synthesis. Current protocols in molecular biology 20020801
The 5,6- and 4,5-benzo derivatives of 1-hydroxy-7-azabenzotriazole. Organic letters 20010906
Properties