39968-33-7 | HOAT 1M DMA solution

Packsize	Purity	Availability	Price	Discounted Price
1g	99%	in stock	$8.00	$5.00
5g	99%	in stock	$13.00	$9.00
10g	99%	in stock	$19.00	$13.00
25g	99%	in stock	$38.00	$26.00
50g	99%	in stock	$73.00	$51.00
100g	99%	in stock	$135.00	$94.00

Description

• Catalog Number: AB43380
• Chemical Name: HOAT 1M DMA solution
• CAS Number: 39968-33-7
• Molecular Formula: C5H4N4O
• Molecular Weight: 136.1115
• MDL Number: MFCD00210053
• SMILES: On1nnc2c1nccc2

Computed Properties

• Complexity: 131
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 10
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.5

Literature

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  Amino acids 20120701

• 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.

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• Design of glycopeptides used to investigate class II MHC binding and T-cell responses associated with autoimmune arthritis.

  PloS one 20110101

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  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.

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  Chemistry (Weinheim an der Bergstrasse, Germany) 20090921

• COMU: a safer and more effective replacement for benzotriazole-based uronium coupling reagents.

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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.

  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

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  Organic letters 20010906