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1,2,3-Trimethoxybenzene

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1,2,3-Trimethoxybenzene Basic information

Product Name:
1,2,3-Trimethoxybenzene
Synonyms:
  • 1,2,3-Trimethoxybenzol
  • Benzene, 1,2,3-trimethoxy-
  • Benzene,1,2,3-trimethoxy-
  • Methylsyringol
  • Tri-O-methylpyrogallol
  • 1,2,3-BENZENETRIOL TRIMETHYL ETHER
  • 1,2,3-trimethyoxy benzene
  • 1,2,3-TRIMETHOXYBENZENE
CAS:
634-36-6
MF:
C9H12O3
MW:
168.19
EINECS:
211-207-2
Product Categories:
  • Benzene derivates
  • Aromatic Hydrocarbons (substituted) & Derivatives
Mol File:
634-36-6.mol
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1,2,3-Trimethoxybenzene Chemical Properties

Melting point:
43-47 °C (lit.)
Boiling point:
241 °C (lit.)
Density 
1.112 g/mL at 25 °C (lit.)
refractive index 
1.5470 (estimate)
Flash point:
>230 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
Chloroform (Slightly), DMSO (Slightly)
form 
Powder
color 
White to dark beige
Water Solubility 
Insoluble in water.
BRN 
1910422
LogP
1.530
CAS DataBase Reference
634-36-6(CAS DataBase Reference)
NIST Chemistry Reference
1,2,3-Trimethoxybenzene(634-36-6)
EPA Substance Registry System
Benzene, 1,2,3-trimethoxy- (634-36-6)
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Safety Information

Risk Statements 
36/37/38
Safety Statements 
22-24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29093090

MSDS

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1,2,3-Trimethoxybenzene Usage And Synthesis

Chemical Properties

WHITE TO DARK BEIGE POWDER

Uses

1,2,3-Trimethoxybenzene can be used for RSM-optimised slow pyrolysis of rice husk for bio-oil production.

Uses

1,2,3-Trimethoxybenzene was used to study the effect of solvent on photoinduced electron-transfer reactions.

Definition

ChEBI: A methoxybenzene that is benzene substituted by methoxy groups at positions 1, 2 and 3 respectively.

General Description

1,2,3-Trimethoxybenzene on condensation with 2,4-diamino-5-(hydroxymethyl)pyrimidine yields 2,4-diamino-5-(2,3,4-trimethoxybenzyl)pyrimidine.

Synthesis

Aqueous sodium hydroxide (40%,150 ml) is added dropwise during3-4 hr to a stirred mixture of pyrogallol (42 g,0.33 mole),sodiumhydrosulphite (10 g,0.057 mole),dimethyl sulphate (146 ml,194.60 g,1.54 mole) kept at 18-22°. Ice (1 kg) is then added and the reactionmixture left overnight. The separated solid is filtered and washed withwater. It is crystallised from methanol as colourless prisms. Yield 37.5 g(66.9%). M.p. 46-47°.Some more product (4 g, 7.1 %) is obtained byextraction of the mother liquor with ether (lit. m.p.46-47°).

Purification Methods

Sublime it under vacuum. [Beilstein 6 H 1081, 6 I 540, 6 II 1066, 6 III 6265, 6 IV 7329.]

1,2,3-Trimethoxybenzene Preparation Products And Raw materials

Preparation Products

Raw materials

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