CAS 15233-65-5 | 2,6-Dimethoxybenzene-1,4-diol | CAS Number 15233-65-5

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15233-65-5 | 2,6-Dimethoxybenzene-1,4-diol

CAS No: 15233-65-5 Catalog No: AG003DOH MDL No:MFCD00017160

Product Description

Catalog Number:

AG003DOH

Chemical Name:

2,6-Dimethoxybenzene-1,4-diol

CAS Number:

15233-65-5

Molecular Formula:

C8H10O4

Molecular Weight:

170.1626

MDL Number:

MFCD00017160

IUPAC Name:

2,6-dimethoxybenzene-1,4-diol

InChI:

InChI=1S/C8H10O4/c1-11-6-3-5(9)4-7(12-2)8(6)10/h3-4,9-10H,1-2H3

InChI Key:

GXAVBFNRWXCOPY-UHFFFAOYSA-N

SMILES:

COc1cc(O)cc(c1O)OC

EC Number:

239-282-7

UNII:

9U2C06A3MM

NSC Number:

49356

Properties

Complexity:

125

Compound Is Canonicalized:

Yes

Covalently-Bonded Unit Count:

Defined Atom Stereocenter Count:

Defined Bond Stereocenter Count:

Exact Mass:

170.058g/mol

Formal Charge:

Heavy Atom Count:

Hydrogen Bond Acceptor Count:

Hydrogen Bond Donor Count:

Isotope Atom Count:

Molecular Weight:

170.164g/mol

Monoisotopic Mass:

170.058g/mol

Rotatable Bond Count:

Topological Polar Surface Area:

58.9A^2

Undefined Atom Stereocenter Count:

Undefined Bond Stereocenter Count:

XLogP3:

0.2

Literature

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Flavonoids and other compounds from Ouratea ferruginea (Ochnaceae) as anticancer and chemopreventive agents.	Molecules (Basel, Switzerland) 20120703
Neuroprotective compounds isolated from Cynanchum paniculatum.	Archives of pharmacal research 20120301
A new phenolic glycoside syringate from the bark of Juglans mandshurica MAXIM. var. sieboldiana MAKINO.	Journal of natural medicines 20090401
Isolation and characterization of bacterial strains Paenibacillus sp. and Bacillus sp. for kraft lignin decolorization from pulp paper mill waste.	The Journal of general and applied microbiology 20081201
Phenolic glycosides from Potalia amara.	Planta medica 20051001
[Isolation and structure elucidation of glycosides in n-butanol extracts from rhizome of Periploca calophylla].	Zhongguo Zhong yao za zhi = Zhongguo zhongyao zazhi = China journal of Chinese materia medica 20050101
Constituents of the stems of Macrococculus pomiferus and their inhibitory activities against cyclooxygenases-1 and -2.	Phytochemistry 20041101