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2,3-Dimethylanisole

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2,3-Dimethylanisole Basic information

Product Name:
2,3-Dimethylanisole
Synonyms:
  • 1-Methoxy-2,3-dimethylbenzene
  • Benzene, 1-methoxy-2,3-dimethyl-
  • 2,3-DIMETHYLANISOLE
  • 2,3-DIMETHYLANISOLE 97%
  • 3-METHOXY-O-XYLENE
  • 1,2-Dimethyl-6-methoxybenzene
  • 2,3-Dimethylphenol methyl ether
  • 1,2-Dimethyl-3-methoxybenzene
CAS:
2944-49-2
MF:
C9H12O
MW:
136.19
EINECS:
220-948-0
Product Categories:
  • Building Blocks
  • C9
  • Chemical Synthesis
  • Organic Building Blocks
  • Oxygen Compounds
  • Ethers
  • Organic Building Blocks
  • Oxygen Compounds
  • Aromatic Ethers
  • Anisoles, Alkyloxy Compounds & Phenylacetates
Mol File:
2944-49-2.mol
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2,3-Dimethylanisole Chemical Properties

Melting point:
29 °C(lit.)
Boiling point:
195 °C(lit.)
Density 
0.984 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.52(lit.)
Flash point:
155 °F
storage temp. 
Inert atmosphere,Room Temperature
form 
powder to lump
Specific Gravity
0.984
color 
White to Almost white
Water Solubility 
immiscible
BRN 
1859736
InChI
InChI=1S/C9H12O/c1-7-5-4-6-9(10-3)8(7)2/h4-6H,1-3H3
InChIKey
BLMBNEVGYRXFNA-UHFFFAOYSA-N
SMILES
C1(OC)=CC=CC(C)=C1C
LogP
3.211 (est)
CAS DataBase Reference
2944-49-2(CAS DataBase Reference)
NIST Chemistry Reference
2,3-Dimethylanisole(2944-49-2)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36-24/25
WGK Germany 
3
HS Code 
29093090

MSDS

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2,3-Dimethylanisole Usage And Synthesis

Chemical Properties

clear light yellow liquid

Uses

2,3-Dimethylanisole is used as starting reagent in the synthesis of biphenyl-indanone A, a positive allosteric modulator of the metabotropic glutamate receptor subtype 2. It can be used to produce 2-methoxy-6-methyl-benzaldehyde by heating.

Synthesis

526-75-0

616-38-6

2944-49-2

General procedure: 1-methoxy-2,3-dimethylbenzene was synthesized by alkylation of 2,3-dimethylphenol with dimethyl carbonate. The specific operation was as follows: 3 mmol of Mn2(CO)10, W(CO)6 or Co2(CO)8 catalyst, 100 mmol of 2,3-dimethylphenol, and 300 mmol of dimethyl carbonate were sequentially added to a 17 mL stainless steel high-pressure microreactor. After sealing the reactor, the reaction was heated at 180 °C for 1 hour. Upon completion of the reaction, the reactor was cooled to room temperature, opened and the reaction mixture was filtered through an alumina layer. The unreacted dimethyl carbonate was removed by distillation, and the residue was distilled under atmospheric or reduced pressure conditions or recrystallized using ethanol to obtain the target product 1-methoxy-2,3-dimethylbenzene. The yield of the reaction was 99% and the boiling point of the product was 95.8-96 °C (30 mmHg).13C NMR data (δC, ppm): 11.99 (CH3), 20.56 (CH3), 55.83 (OCH3), 110.02 (C6), 122.43 (C4), 124.78 (C2), 128.74 (C5). 137.70 (C3), 157.36 (C1). Elemental analysis results (measured values): C 79.29%, H 8.82%; calculated values for molecular formula C9H12O: C 79.37%, H 8.88%.

References

[1] Russian Journal of Organic Chemistry, 2015, vol. 51, # 3, p. 330 - 334
[2] Methylation of Phenol and Its Derivatives with Dimethyl Carbonate in the Presence of Mn2(CO)10, W(CO)6, and Co2(CO)8, 2015, vol. 51, # 3, p. 330 - 334,5

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