608-25-3

  • Product Name:2-METHYLRESORCINOL
  • Molecular Formula:C7H8O2
  • Purity:99%
  • Molecular Weight:124.139
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Product Details;

CasNo: 608-25-3

Molecular Formula: C7H8O2

Appearance: White to off-white crystal powder

Hot Sale Quality Factory Supply 2-METHYLRESORCINOL 608-25-3 Cheapest Price

  • Molecular Formula:C7H8O2
  • Molecular Weight:124.139
  • Appearance/Colour:White to off-white crystal powder 
  • Vapor Pressure:0.00201mmHg at 25°C 
  • Melting Point:114-120 °C(lit.) 
  • Refractive Index:1.594 
  • Boiling Point:282.1 °C at 760 mmHg 
  • PKA:pK1:10.05;pK2:11.64 (25°C,μ=0.65) 
  • Flash Point:142.9 °C 
  • PSA:40.46000 
  • Density:1.21 g/cm3 
  • LogP:1.40620 

2-Methylresorcinol(Cas 608-25-3) Usage

Chemical Properties

White to off-white crystal powder

Uses

2-Methylresorcinol is used in the preparation of aromatic benziporphyrins, tripyrrane analogs and C-5-bromo-2-hydroxyphenylcalix[4]-2-methylresorcinarene. Further, it is employed in oxidative and non-oxidative hair dye formulations.

Application

2-Methylresorcinol is used as medicine, pesticide, dye intermediate, hair auxiliaries, etc.

Preparation

Synthesis of 2-methylresorcinol: The synthetic routes to an alkylresorcinol that is partially alkylated at a position other than the 4th position on the aromatic ring are multistep and give low overall yields. For example, a 50% yield of a 2-methylresorcinol is obtained by hydrogenation of resorcinol and methylation of the resulting dihydroresorcinol to 2-methylcyclohexane-1,3-dione which on treatment with bromine is converted into 4,6-dibromo-2-methylresorcinol and finally hydrogenolysis of the dibromo derivative to produce the 2-methylresorcinol. Another example is that 5-methylresorcinol can be prepared by a five-step synthesis starting with p-toluidine or a four-step synthesis starting from ethyl crotonate. The five-step synthesis involves acetylation, two-step nitration, reductive hydrogenation, and hydrolysis.Literature source US04086281

General Description

The reaction between 2-methylresorcinol and 2-alkenals was studied to investigate the scavenging ability of m-diphenols for the 2-alkenals formed during lipid oxidation.

Flammability and Explosibility

Nonflammable

InChI:InChI=1/C7H8O2/c1-5-6(8)3-2-4-7(5)9/h2-4,8-9H,1H3

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608-25-3 Process route

methanol
67-56-1

methanol

recorcinol
108-46-3

recorcinol

O-methylresorcine
150-19-6

O-methylresorcine

4-methyl resorcinol
496-73-1,73073-80-0

4-methyl resorcinol

2-methylbenzene-1,3-diol
608-25-3

2-methylbenzene-1,3-diol

1,3-Dimethoxybenzene
151-10-0

1,3-Dimethoxybenzene

Conditions
Conditions Yield
With lanthanum phosphate-alumina; at 290 ℃; Temperature; Reagent/catalyst; Inert atmosphere;
 
ortho-cresol
95-48-7,77504-84-8

ortho-cresol

4-methyl resorcinol
496-73-1,73073-80-0

4-methyl resorcinol

2-methylbenzene-1,4-diol
95-71-6,96937-50-7

2-methylbenzene-1,4-diol

2-methylbenzene-1,3-diol
608-25-3

2-methylbenzene-1,3-diol

3-methylbenzene-1,2-diol
488-17-5

3-methylbenzene-1,2-diol

Conditions
Conditions Yield
With hydrogen fluoride; dihydrogen peroxide; antimony pentafluoride; at -40 ℃; for 0.5h; Product distribution;
17%
4%
3%
3%
With hydrogen fluoride; dihydrogen peroxide; antimony pentafluoride; at -40 ℃; for 0.5h;
17%
3%
3%
4%

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