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Home Other Building Blocks 1,4-Benzenediol, 2,5-dimethoxy-

1,4-Benzenediol, 2,5-dimethoxy-

CAS No.:
13239-13-9
Catalog Number:
AG0010N2
Molecular Formula:
C8H10O4
Molecular Weight:
170.1626
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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
Properties