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13239-13-9

13239-13-9 | 1,4-Benzenediol, 2,5-dimethoxy-

CAS No: 13239-13-9 Catalog No: AG0010N2 MDL No:MFCD24713419

Product Description

Catalog Number:
AG0010N2
Chemical Name:
1,4-Benzenediol, 2,5-dimethoxy-
CAS Number:
13239-13-9
Molecular Formula:
C8H10O4
Molecular Weight:
170.1626
MDL Number:
MFCD24713419
IUPAC Name:
2,5-dimethoxybenzene-1,4-diol
InChI:
InChI=1S/C8H10O4/c1-11-7-3-6(10)8(12-2)4-5(7)9/h3-4,9-10H,1-2H3
InChI Key:
GLJCPHKWYYCHCQ-UHFFFAOYSA-N
SMILES:
COc1cc(O)c(cc1O)OC
NSC Number:
139147

Properties

Complexity:
123  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
170.058g/mol
Formal Charge:
0
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Isotope Atom Count:
0
Molecular Weight:
170.164g/mol
Monoisotopic Mass:
170.058g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
58.9A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.2  

Literature

Title Journal
Neuroprotective compounds isolated from Cynanchum paniculatum. Archives of pharmacal research 20120301
Multiple multi-copper oxidase gene families in basidiomycetes - what for? Current genomics 20110401
Ozonolysis of lignin models in aqueous solution: anisole, 1,2-dimethoxybenzene, 1,4-dimethoxybenzene, and 1,3,5-trimethoxybenzene. Environmental science & technology 20090815
Fungal hydroquinones contribute to brown rot of wood. Environmental microbiology 20061201
Degradation of 2-fluorophenol by the brown-rot fungus Gloeophyllum striatum: evidence for the involvement of extracellular Fenton chemistry. Applied microbiology and biotechnology 20040401
Significant levels of extracellular reactive oxygen species produced by brown rot basidiomycetes on cellulose. FEBS letters 20021120

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