1916-07-0

  • Product Name:3,4,5-Trimethoxybenzoic acid methyl ester
  • Molecular Formula:C11H14O5
  • Purity:99%
  • Molecular Weight:226.229
Inquiry

Product Details

pd_meltingpoint:81-85 °C

Appearance:white to light yellow powder

Chinese factory supply 3,4,5-Trimethoxybenzoic acid methyl ester 1916-07-0 in stock with high standard

  • Molecular Formula:C11H14O5
  • Molecular Weight:226.229
  • Appearance/Colour:white to light yellow powder 
  • Vapor Pressure:0.00538mmHg at 25°C 
  • Melting Point:81-85 °C 
  • Refractive Index:1.494 
  • Boiling Point:274.5 °C at 760 mmHg 
  • Flash Point:115.2 °C 
  • PSA:53.99000 
  • Density:1.134 g/cm3 
  • LogP:1.49900 

Methyl 3,4,5-trimethoxybenzoate(Cas 1916-07-0) Usage

InChI:InChI=1/C11H14O5/c1-13-8-5-7(11(12)16-4)6-9(14-2)10(8)15-3/h5-6H,1-4H3

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1916-07-0 Process route

3,4-Dihydroxybenzoic acid
99-50-3

3,4-Dihydroxybenzoic acid

4-hydroxysalicylic acid
89-86-1

4-hydroxysalicylic acid

3,4,5-trihydroxybenzoic acid
149-91-7

3,4,5-trihydroxybenzoic acid

3,5-Dihydroxybenzoic acid
99-10-5

3,5-Dihydroxybenzoic acid

2,3-Dihydroxybenzoic acid
303-38-8

2,3-Dihydroxybenzoic acid

2,5-dihydroxybenzoic acid.
490-79-9

2,5-dihydroxybenzoic acid.

3-Carboxyphenol
99-06-9

3-Carboxyphenol

salicylic acid
69-72-7,25496-36-0,8052-31-1

salicylic acid

methyl iodide
74-88-4

methyl iodide

4-hydroxy-benzoic acid
99-96-7

4-hydroxy-benzoic acid

methyl 2, 4-dimethoxybenzoate
2150-41-6

methyl 2, 4-dimethoxybenzoate

2-methoxybenzoic acid methyl ester
606-45-1

2-methoxybenzoic acid methyl ester

methyl 3-methoxybenzoate
5368-81-0

methyl 3-methoxybenzoate

methyl 4-methoxybenzoate
121-98-2

methyl 4-methoxybenzoate

methyl 3,4-dimethoxybenzoate
2150-38-1

methyl 3,4-dimethoxybenzoate

3,4,5-trimethoxybenzoic acid methyl ester
1916-07-0

3,4,5-trimethoxybenzoic acid methyl ester

methyl 2,3-dimethoxybenzoate
2150-42-7

methyl 2,3-dimethoxybenzoate

methyl 2,5-dimethoxybenzoate
2150-40-5

methyl 2,5-dimethoxybenzoate

methyl 3,5-dimethoxybenzoate
2150-37-0

methyl 3,5-dimethoxybenzoate

Conditions
Conditions Yield
3,4-Dihydroxybenzoic acid; 4-hydroxysalicylic acid; 3,4,5-trihydroxybenzoic acid; 3,5-Dihydroxybenzoic acid; 2,3-Dihydroxybenzoic acid; 2,5-dihydroxybenzoic acid.; 3-Carboxyphenol; salicylic acid; 4-hydroxy-benzoic acid; With sodium hydride; In hexane; N,N-dimethyl-formamide; at 25 ℃; for 2h; Inert atmosphere; Cooling with ice;
methyl iodide; In hexane; N,N-dimethyl-formamide; for 72h; Inert atmosphere;
diazomethane
186581-53-3,908094-01-9,334-88-3

diazomethane

C<sub>66</sub>H<sub>68</sub>O<sub>31</sub>

C66H68O31

alpha-D-glucopyranose
492-62-6

alpha-D-glucopyranose

3,4,5-trimethoxybenzoic acid methyl ester
1916-07-0

3,4,5-trimethoxybenzoic acid methyl ester

dimethyl (S)-4,4',5,5',6,6'-hexamethoxydiphenoate
4891-62-7,65995-60-0,71307-89-6

dimethyl (S)-4,4',5,5',6,6'-hexamethoxydiphenoate

3-(2,3-Dimethoxy-5-methoxycarbonyl-phenoxy)-4,5,6,4',5',6'-hexamethoxy-biphenyl-2,2'-dicarboxylic acid dimethyl ester
82203-13-2,98899-87-7

3-(2,3-Dimethoxy-5-methoxycarbonyl-phenoxy)-4,5,6,4',5',6'-hexamethoxy-biphenyl-2,2'-dicarboxylic acid dimethyl ester

Conditions
Conditions Yield
With sodium hydroxide; Yield given. Multistep reaction; 1.) MeOH, reflux, 2.5 h, 2.) ether, 30 min;
With sodium hydroxide; Yield given. Multistep reaction. Yields of byproduct given; 1.) MeOH, reflux, 2.5 h, 2.) ether, 30 min;

1916-07-0 Upstream products

  • 186581-53-3
    186581-53-3

    diazomethane

  • 24093-81-0
    24093-81-0

    methyl 3,5-dihydroxy-4-methoxybenzoate

  • 118-41-2
    118-41-2

    Eudesmic acid

  • 623-11-0
    623-11-0

    1-methyl-4-nitrosobenzene

1916-07-0 Downstream products

  • 101275-75-6
    101275-75-6

    (piperidine-1-carbonyl)-(3,4,5-trimethoxy-benzoyl)-amine

  • 858468-00-5
    858468-00-5

    1,2,3-trimethoxy-5-(prop-1-en-2-yl)benzene

  • 267003-32-7
    267003-32-7

    3-(3,4,5-trimethoxyphenyl)-3-pentanol

  • 1968-71-4
    1968-71-4

    methyl 2-bromo-3,4,5-trimethoxybenzoate

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