3,5-Dimethoxytoluene

3,5-Dimethoxytoluene Basic information
Product Name:3,5-Dimethoxytoluene
Synonyms:3,5-DIMETHOXYTOLUENE;3,5-DiMethoxytoluene, GC 98%;ORCINOL DIMETHYL ETHER;3,5-Dimethoxy-1-methylbenzene;5-Methylresorcinol dimethyl ether;Benzene, 1,3-dimethoxy-5-methyl-;Toluene, 3,5-dimethoxy-;1,5-Dimethoxy-3-methylbenzene
CAS:4179-19-5
MF:C9H12O2
MW:152.19
EINECS:224-048-9
Product Categories:Building Blocks;C9;Aromatic Ethers;Ethers;Organic Building Blocks;Oxygen Compounds;Chemical Synthesis;Organic Building Blocks;Oxygen Compounds
Mol File:4179-19-5.mol
3,5-Dimethoxytoluene Structure
3,5-Dimethoxytoluene Chemical Properties
Melting point 61-62 C
Boiling point 244 °C (lit.)
density 1.039 g/mL at 25 °C (lit.)
refractive index n20/D 1.522(lit.)
Fp 215 °F
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Sparingly), Methanol (Sparingly)
form Liquid
Specific Gravity1.039
color Clear colorless to yellow
BRN 2043558
LogP2.897 (est)
CAS DataBase Reference4179-19-5(CAS DataBase Reference)
NIST Chemistry Reference3,5-Dimethoxytoluene(4179-19-5)
EPA Substance Registry System3,5-Dimethoxytoluene (4179-19-5)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
TSCA Yes
HS Code 29093090
MSDS Information
ProviderLanguage
SigmaAldrich English
ALFA English
3,5-Dimethoxytoluene Usage And Synthesis
Chemical PropertiesClear colorless to yellow liquid
Uses3,5-Dimethoxytoluene (DMT) may be used in the synthesis of 3,5-dimethoxybenzoic acid by oxidation and 2-methoxy-6-methyl-1,4-benzoquinone by catalytic oxidation with hydrogen peroxide (H2O2)/methyltrioxorhenium (CH3ReO3) in dimethyl carbonate (DMC).
DefinitionChEBI: 3,5-dimethoxytoluene is a member of the class of toluenes that is toluene in which the hydrogens at positions 3 and 5 have been replaced by methoxy groups. It is the major scent compound of many rose varieties. It has a role as a fragrance and a plant metabolite. It is a member of toluenes and a member of methoxybenzenes.
Synthesis Reference(s)Organic Syntheses, Coll. Vol. 6, p. 859, 1988
The Journal of Organic Chemistry, 70, p. 3275, 2005 DOI: 10.1021/jo050075r
General Description3,5-Dimethoxytoluene (DMT) is a methoxylated phenolic derivative. It is reported to be one of the main constituent of the floral volatiles in different rose varieties. It has been biosynthesized from orcinol by two successive methylation catalyzed by O-methyltransferases (OMTs). The features of its aerobic oxidation with metal/bromide catalysts have been investigated.
4-IODO-2,5-DIMETHOXYTOLUENE 2,4-DIMETHOXYTOLUENE,2,4-Dimethoxy-1-methylbenzene alpha-chloro-3,4-dimethoxytoluen 2-BROMO-3,5-DIMETHOXYTOLUENE 4-HYDROXY-3,5-DIMETHOXYTOLUENE 1,4-DIHYDROXY-2,3-DIMETHOXY-5-METHYLBENZENE BENZALDEHYDE DIMETHYL ACETAL, (A,A-DIMETHOXYTOLUENE) 3,4-dihydro-5,6,7-trimethoxy-2-naphthoic acid 1-ACETYL-2,5-DIMETHOXY-4-METHYLBENZENE 3,4,5-Trimethoxybenzyl alcohol 3,5-DIMETHOXYCINNAMIC ACID ammonium alpha-hydroxy-3,4-dimethoxytoluene-alpha-sulphonate sodium alpha-hydroxy-3,4-dimethoxytoluene-alpha-sulphonate 2,6-DIMETHOXYTOLUENE,1,3-Dimethoxy-2-methylbenzene 4-ETHOXYCARBONYLOXY-3,5-DIMETHOXYBENZOIC ACID 1-(CHLOROMETHYL)-4,5-DIMETHOXY-2-METHYLBENZENE 1-BROMO-3,4-DIMETHOXY-2-METHYLBENZENE 1-BROMO-2,5-DIMETHOXY-4-METHYLBENZENE,4-BROMO-2,5-DIMETHOXYTOLUENE

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