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Factory supply Methyl 3-methoxysalicylate 6342-70-7 with sufficient production capacity

  • Molecular Formula: C9H10O4
  • Molecular Weight: 182.176
  • Vapor Pressure: 0.00975mmHg at 25°C 
  • Melting Point: 65-68 °C(lit.) 
  • Refractive Index: 1.534 
  • Boiling Point: 256.1 °C at 760 mmHg 
  • PKA: 9.76±0.10(Predicted) 
  • Flash Point: 97.8 °C 
  • PSA: 55.76000 
  • Density: 1.216 g/cm3 
  • LogP: 1.18740 

Methyl 3-methoxysalicylate(Cas 6342-70-7) Usage

General Description

Methyl 3-methoxysalicylate is an organic compound that is commonly used in the fragrance and flavor industry. It is a clear, colorless liquid with a sweet, floral odor. This chemical is often used as a fragrance ingredient in various personal care products, such as perfumes, lotions, and shampoo. It is also used as a flavoring agent in food products and as an additive in industrial and household products. Methyl 3-methoxysalicylate is synthesized through the esterification of 3-methoxysalicylic acid with methanol, and it is known for its strong and long-lasting aroma.

InChI:InChI=1/C9H10O4/c1-12-7-5-3-4-6(8(7)10)9(11)13-2/h3-5,10H,1-2H3

6342-70-7 Relevant articles

Phosphorescence at Low Temperature by External Heavy-Atom Effect in Zinc(II) Clusters

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, p. 5875 - 5879 (2019)

Luminescent ZnII clusters [Zn4L4(μ3-OMe)...

Evaluation of novel N′-(3-hydroxybenzoyl)-2-oxo-2H-chromene-3-carbohydrazide derivatives as potential HIV-1 integrase inhibitors

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Choleretic drug alibendol preparation method

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Paragraph 0017; 0020, (2019/06/30)

The invention belongs to the field of dr...

Pharmaceutical composition for use in preventing or treating poly(ADP-ribose)polymerase-1 related diseases containing the same as an active ingredient

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Paragraph 0441; 0453-0455, (2018/06/29)

The present invention relates to a novel...

6342-70-7 Process route

methanol
67-56-1

methanol

3-methoxysalicylic acid
877-22-5

3-methoxysalicylic acid

3-methoxymethylsalicylate
6342-70-7

3-methoxymethylsalicylate

Conditions
Conditions Yield
With hydrogenchloride; for 2h; Heating;
98%
With sulfuric acid; for 16h; Reflux;
96%
With sulfuric acid; for 48h; Heating;
95%
With sulfuric acid; for 24h; Heating;
94%
With sulfuric acid; for 58h; Heating;
92%
sulfuric acid; for 96h; Heating / reflux;
91.2%
With sulfuric acid; for 28h; Heating;
70%
With dicyclohexyl-carbodiimide; In tetrahydrofuran; at 20 ℃;
62%
With sulfuric acid;
With hydrogenchloride;
With hydrogenchloride; at 20 ℃;
With thionyl chloride; Heating;
With sulfuric acid; at 0 ℃; Reflux;
1.15 g
With sulfuric acid; for 16h; Reflux;
With sulfuric acid; for 24h; Reflux;
3-methoxysalicylic acid
877-22-5

3-methoxysalicylic acid

3-methoxymethylsalicylate
6342-70-7

3-methoxymethylsalicylate

Conditions
Conditions Yield
With methanol; sulfuric acid; In methanol; for 96h;
91.2%

6342-70-7 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 877-22-5
    877-22-5

    3-methoxysalicylic acid

  • 67-56-1
    67-56-1

    methanol

  • 2150-42-7
    2150-42-7

    methyl 2,3-dimethoxybenzoate

6342-70-7 Downstream products

  • 134419-43-5
    134419-43-5

    5-bromo-2-hydroxy-3-methoxy-benzoic acid methyl ester

  • 134419-45-7
    134419-45-7

    2-methoxy-6-methoxycarbonyl-4-nitrophenol

  • 500798-31-2
    500798-31-2

    2-acetoxy-3-methoxy-benzoic acid methyl ester

  • 96619-89-5
    96619-89-5

    3-methoxy-2-(2-propenyloxy)benzoic acid, methyl ester

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