3,4-Dimethoxyphenol - CAS 2033-89-8

Catalog:	BB015817
Product Name:	3,4-Dimethoxyphenol
CAS:	2033-89-8
Synonyms:	3,4-dimethoxyphenol
Application:	A substituted alkynyl phenoxy compound as new synergists in pesticidal compositions.

Technical Data

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Computed Properties

IUPAC Name:	3,4-dimethoxyphenol
Description:	3,4-Dimethoxyphenol is a natural phenol found in the herbs of Tripterygium wilfordii.
Molecular Weight:	154.16
Molecular Formula:	C8H10O3
Canonical SMILES:	COC1=C(C=C(C=C1)O)OC
InChI:	InChI=1S/C8H10O3/c1-10-7-4-3-6(9)5-8(7)11-2/h3-5,9H,1-2H3
InChI Key:	SMFFZOQLHYIRDA-UHFFFAOYSA-N
Boiling Point:	271.2 ℃
Purity:	> 98 %
Density:	1.134 g/cm³
Appearance:	Oil
MDL:	MFCD00008390
LogP:	1.40940
Quality Standard:	Enterprise Standard

Publication Number	Title	Priority Date
CN-113308497-A	Method for improving biogas production efficiency and gas production rate of lignocellulose raw material through anaerobic digestion	20210706
CN-113121485-A	3-aryl coumarin derivative and preparation method and application thereof	20210301
CN-112876354-A	2- (4-methoxyphenoxy) propionic acid derivative with sweet taste inhibiting effect and industrial production method thereof	20210208
CN-112320766-A	Preparation method and application of hollow mesoporous inorganic oxide nanosphere solid base	20201113
CN-112225744-A	6H-benzopyrano [3,4-b ] quinoline compound and preparation method and application thereof	20200831

PMID	Publication Date	Title	Journal
23124346	20121101	Kinetic properties of manganese peroxidase from the mushroom Stereum ostrea and its ability to decolorize dyes	Journal of microbiology and biotechnology
22866699	20120815	Flocculation and haze removal from crude beer using in-house produced laccase from Trametes versicolor cultured on brewer's spent grain	Journal of agricultural and food chemistry
22328260	20120701	Decolorization and biodegradation of Rubine GFL by microbial consortium GG-BL in sequential aerobic/microaerophilic process	Applied biochemistry and biotechnology
22161298	20120601	Bacterial assisted phytoremediation for enhanced degradation of highly sulfonated diazo reactive dye	Environmental science and pollution research international
22520499	20120601	Phytochemicals to suppress Fusarium head blight in wheat-chickpea rotation	Phytochemistry

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Related Functional Groups

Oxygen Compounds

[134769-80-5]
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[1427004-19-0]
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[52378-69-5]
Diethyl trans-cinnamylphosphonate
[1006443-01-1]
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid
[865774-78-3]
2-(6,8-difluoro-1,2,3,4-tetrahydro-naphthalen-2-ylamino)-pentanoic acid methyl ester
[2960-93-2]
2,2'-Dimethoxy-1,1'-binaphthalene

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GHS Hazard Statement:	H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]
Precautionary Statement:	P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501
Signal Word:	Warning

Complexity:	116
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	1
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	154.062994177
Formal Charge:	0
Heavy Atom Count:	11
Hydrogen Bond Acceptor Count:	3
Hydrogen Bond Donor Count:	1
Isotope Atom Count:	0
Monoisotopic Mass:	154.062994177
Rotatable Bond Count:	2
Topological Polar Surface Area:	38.7 Å²
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0
XLogP3:	1.7