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163857-09-8

163857-09-8 | 2,5-Furandicarboxaldehyde, radical ion(1-) (9CI)

CAS No: 163857-09-8 Catalog No: AG00B13X MDL No:

Product Description

Catalog Number:
AG00B13X
Chemical Name:
2,5-Furandicarboxaldehyde, radical ion(1-) (9CI)
CAS Number:
163857-09-8
IUPAC Name:
furan-2,5-dicarbaldehyde
InChI:
InChI=1S/C6H4O3/c7-3-5-1-2-6(4-8)9-5/h1-4H
InChI Key:
PXJJKVNIMAZHCB-UHFFFAOYSA-N
EC Number:
212-520-7
UNII:
L4HT8N2Z72
NSC Number:
618088

Properties

Complexity:
108  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
124.016g/mol
Formal Charge:
0
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
124.095g/mol
Monoisotopic Mass:
124.016g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
47.3A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.6  

Literature

Title Journal
Discovery and characterization of a 5-hydroxymethylfurfural oxidase from Methylovorus sp. strain MP688. Applied and environmental microbiology 20140201
Thermal decomposition of 5-(hydroxymethyl)-2-furaldehyde (HMF) and its further transformations in the presence of glycine. Journal of agricultural and food chemistry 20110928
Efficient aerobic oxidation of 5-hydroxymethylfurfural to 2,5-diformylfuran, and synthesis of a fluorescent material. ChemSusChem 20110117
2,25-Dioxo-27,28-diphenyl-30-oxa-29-thia-3,10,17,24-tetra-aza-penta-cyclo-[24.2.1.1.0.0]triaconta-5,7,9(4),10,12,14,16,18,20,22,26,28-dodeca-ene chloro-form disolvate. Acta crystallographica. Section E, Structure reports online 20100301
Improved method to measure aldehyde adducts to N-terminal valine in hemoglobin using 5-hydroxymethylfurfural and 2,5-furandialdehyde as model compounds. Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 20090801
Synthesis, spectroscopy, and reactivity of meso-unsubstituted azuliporphyrins and their heteroanalogues. Oxidative ring contractions to carba-, oxacarba-, thiacarba-, and selenacarbaporphyrins. The Journal of organic chemistry 20041210
Oxidation of heterocyclic and aromatic aldehydes to the corresponding carboxylic acids by Acetobacter and Serratia strains. Biotechnology letters 20041101
Kinetic versus thermodynamic control during the formation of [2]rotaxanes by a dynamic template-directed clipping process. Chemistry (Weinheim an der Bergstrasse, Germany) 20030905
One-pot, two-step, practical catalytic synthesis of 2,5-diformylfuran from fructose. Organic letters 20030529

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