ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatic alcohol 2,3-Dimethoxyphenol

2,3-Dimethoxyphenol

2,3-Dimethoxyphenol Basic information
Product Name:2,3-Dimethoxyphenol
Synonyms:2,3-DIMETHOXYPHENOL;PYROGALLOL-1,2-DIMETHYL ETHER;Phenol, 2,3-dimethoxy-;1-Hydroxy-2,3-dimethoxybenzene;2,3-Dimethoxyphenol 96%;2,3-Dimethoxyphenol,99%;2,3-Dimethoxyphenol, typically 98%;2,3-DiMethoxyphenol, 99% 5GR
CAS:5150-42-5
MF:C8H10O3
MW:154.16
EINECS:225-922-2
Product Categories:Aromatic Phenols
Mol File:5150-42-5.mol
2,3-Dimethoxyphenol Structure
2,3-Dimethoxyphenol Chemical Properties
Boiling point 233-234 °C (lit.)
density 1.182 g/mL at 25 °C (lit.)
refractive index n20/D 1.539(lit.)
Fp 228 °F
storage temp. 2-8°C
solubility Soluble in Chloroform.
form Liquid
pka9.59±0.10(Predicted)
color Clear orange to brown
BRN 1910045
LogP1.143 (est)
CAS DataBase Reference5150-42-5(CAS DataBase Reference)
NIST Chemistry Reference2,3-Dimethoxyphenol(5150-42-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-37/39-37
WGK Germany 3
Hazard Note Irritant
HS Code 29095000
MSDS Information
ProviderLanguage
2,3-Dimethoxyphenol English
SigmaAldrich English
ACROS English
ALFA English
2,3-Dimethoxyphenol Usage And Synthesis
Chemical PropertiesCLEAR ORANGE TO BROWNISH LIQUID
Uses2,3-Dimethoxyphenol has been used to study the nitrosative deamination of DNA bases induced by reactive nitrogen species (RNS) while studying the cause of mutagenesis.
Uses2,3-Dimethoxyphenol is used to study the nitrosative deamination of DNA bases induced by reactive nitrogen species (RNS) while studying the cause of mutagenesis.
DefinitionChEBI: 2,3-dimethoxyphenol is a member of phenols and a member of methoxybenzenes.
General Description2,3-Dimethoxyphenol is a plant-derived phenylpropanoid compound that is glycosidated to form glycoside compound.
2,3-Dimethoxyphenol Preparation Products And Raw materials
Preparation Products2'-HYDROXY-3',4'-DIMETHOXYACETOPHENONE-->2,3-Dimethoxy-5-methyl-1,4-hydroquinone-->7,8-Dimethoxy-4-methyl-chromen-2-one-->Phenol, 6-broMo-2,3-diMethoxy--->1,3,2-Dioxaborolane, 2-[3,4-dimethoxy-2-(phenylmethoxy)phenyl]-4,4,5,5-tetramethyl--->Benzaldehyde, 2-ethoxy-3,4-dimethoxy- (9CI)
2,5-Dimethoxyphenol 2,6-Dimethoxyphenol 4-{[(4-hydroxycyclohexyl)amino]methyl}-2,6-dimethoxyphenol 2,4-Dimethoxyphenol acetate 4-[3-(2-Methylmorpholino)-3-oxo-1-propenyl]-2,6-dimethoxyphenol 4-{[(4-bromophenyl)amino]methyl}-2,6-dimethoxyphenol 4-[(E)-3-Hydroxy-1-propenyl]-2,6-dimethoxyphenol 3,4-dihydro-5,6,7-trimethoxy-2-naphthoic acid 4-[(Z)-3-Hydroxy-1-propenyl]-2,6-dimethoxyphenol 4-{[(4-ethylphenyl)amino]methyl}-2,6-dimethoxyphenol 4-{[(5-chloro-2-methylphenyl)amino]methyl}-2,6-dimethoxyphenol METHOXYPHENOL, PARA-(SG) 4-{[(4-iodophenyl)amino]methyl}-2,6-dimethoxyphenol 3,3'-[(2S,3R)-2,3-Dimethyl-1,4-butanediyl]bis(5,6-dimethoxyphenol),3,3'-[(2R,3S)-2,3-Dimethyl-1,4-butanediyl]bis(5,6-dimethoxyphenol) 1,1-Dimethoxyethane 4-[(E)-2-(2-Thienyl)ethenyl]-2,6-dimethoxyphenol 3,5-Dimethoxyphenol acetate 4,4'-(2,3-Dimethylbutane-1,4-diyl)bis(2,6-dimethoxyphenol)
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