Catalog No.:AA002OUG

24645-80-5 | 4-Hydroxyphenyl glyoxal

Name: Name:4-Hydroxyphenyl glyoxal
Brand: AABLOCKS
SKU: AA002OUG
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25mg

≥ 99% (NMR)

in stock

$162.00 $114.00

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100mg

≥ 99% (NMR)

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$310.00 $217.00

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Technical Information
Properties
Downstream Synthesis Route
Literature
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Technical Information
Properties
Downstream Synthesis Route
Literature

Technical Information

Catalog Number:

AA002OUG

Chemical Name:

4-Hydroxyphenyl glyoxal

CAS Number:

24645-80-5

Molecular Formula:

C8H6O3

Molecular Weight:

150.1314

MDL Number:

MFCD00054984

SMILES:

O=CC(=O)c1ccc(cc1)O

NSC Number:

145743

Properties

Form:

Solid

Storage:

-20 ℃;Inert atmosphere;

Computed Properties

Complexity:

157

Covalently-Bonded Unit Count:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Rotatable Bond Count:

XLogP3:

1.4

Downstream Synthesis Route

24645-80-5

53673-01-1

56442-94-5

[1]Barlow;Main;Snow[JournalofMedicinalChemistry,1981,vol.24,#3,p.315-322]

24645-80-5

108784-42-5

6-fluoro-3-hydroxy-2-(4'-hydroxyphenyl)imidazo<1,2-b>pyridazine

[1]AustralianJournalofChemistry,1994,vol.47,p.609-622

24645-80-5

49721-45-1

677297-48-2

[1]Patent:US2005/282814,2005,A1

Literature

Title: Revealing a positive charge patch on a recombinant monoclonal antibody by chemical labeling and mass spectrometry.

Journal: Analytical chemistry 20111115

Title: Cross-talk between the catalytic core and the regulatory domain in cystathionine β-synthase: study by differential covalent labeling and computational modeling.

Journal: Biochemistry 20101214

Title: A technique for the specific enrichment of citrulline-containing peptides.

Journal: Analytical biochemistry 20100801

Title: Probing the ligand-induced conformational change in HLA-DR1 by selective chemical modification and mass spectrometric mapping.

Journal: Biochemistry 20051025

Title: Alteration of substrate selectivity through mutation of two arginine residues in the binding site of amadoriase II from Aspergillus sp.

Journal: Biochemistry 20020402

Title: Ligand-selective modulation of the permeability transition pore by arginine modification. Opposing effects of p-hydroxyphenylglyoxal and phenylglyoxal.

Journal: The Journal of biological chemistry 20020111

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