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Manufacturer supply 2,3,4-Trimethoxybenzoic acid 573-11-5 with sufficient stock and high standard

  • Molecular Formula: C10H12O5
  • Molecular Weight: 212.202
  • Appearance/Colour: off-white crystalline powder 
  • Vapor Pressure: 0.000127mmHg at 25°C 
  • Melting Point: 99-102 °C(lit.) 
  • Refractive Index: 1.5140 (estimate) 
  • Boiling Point: 321 °C at 760 mmHg 
  • PKA: 4.24±0.10(Predicted) 
  • Flash Point: 123.5 °C 
  • PSA: 64.99000 
  • Density: 1.219 g/cm3 
  • LogP: 1.41060 

2,3,4-Trimethoxybenzoic acid(Cas 573-11-5) Usage

InChI:InChI=1/C10H12O5/c1-13-7-5-4-6(10(11)12)8(14-2)9(7)15-3/h4-5H,1-3H3,(H,11,12)/p-1

573-11-5 Relevant articles

Total synthesis and RXRα-mediated transcription studies of neriifolone B and related compounds

Shen, Qirong,Dai, Yi,Wang, Guanghui,Yao, Fei,Duan, Yinghui,Chen, Haifeng,Zhang, Weige,Zhang, Xiaokun,Yao, Xinsheng

, p. 2671 - 2677 (2014/05/06)

Neriifolone B (1), a natural product con...

NbCl5 mediated deprotection of methoxy methyl ether

Yadav,Ganganna,Bhunia, Dinesh C.,Srihari

experimental part, p. 4318 - 4320 (2009/10/26)

An efficient cleavage of methoxy methyl ...

CuCl catalyzed oxidation of aldehydes to carboxylic acids with aqueous tert-butyl hydroperoxide under mild conditions

Mannam, Sreedevi,Sekar

, p. 1083 - 1086 (2008/09/18)

Oxidation of aldehydes to the correspond...

Efficient and rapid method for the oxidation of electron-rich aromatic aldehydes to carboxylic acids using improved basic hydrogen peroxide

Cong, Zhi-Qi,Wang, Chun-Ian,Chen, Tie,Yin, Bing-Zhu

, p. 679 - 683 (2007/10/03)

An efficient and rapid method for oxidat...

573-11-5 Process route

2,3,4-trimethoxybenzaldehyde
2103-57-3

2,3,4-trimethoxybenzaldehyde

2,3,4-Trimethoxy-benzoic acid
573-11-5

2,3,4-Trimethoxy-benzoic acid

Conditions
Conditions Yield
With dihydrogen peroxide; potassium hydroxide; In methanol; water; for 8.5h; Reflux;
95%
With tert.-butylhydroperoxide; copper(l) chloride; In acetonitrile; at 20 ℃; for 2h;
91%
With permanganate(VII) ion;
With potassium hydroxide; dihydrogen peroxide; In methanol; water; Heating;
C<sub>12</sub>H<sub>16</sub>O<sub>6</sub>
1178514-38-9

C12 H16 O6

2,3,4-Trimethoxy-benzoic acid
573-11-5

2,3,4-Trimethoxy-benzoic acid

Conditions
Conditions Yield
With niobium pentachloride; In acetonitrile; at 0 - 20 ℃; for 1h;
93%

573-11-5 Upstream products

  • 634-36-6
    634-36-6

    1,2,3-trimethoxybenzene

  • 13909-73-4
    13909-73-4

    2',3',4'-trimethoxyacetophenone

  • 6395-18-2
    6395-18-2

    methyl 2,3,4-trimethoxybenzoate

  • 4082-16-0
    4082-16-0

    2',3',4'-trimethoxychalcone

573-11-5 Downstream products

  • 64059-58-1
    64059-58-1

    (trimethoxy-2,3,4 phenyl) (morpholino-4)methanone

  • 125928-15-6
    125928-15-6

    (2-Thioxo-thiazolidin-3-yl)-(2,3,4-trimethoxy-phenyl)-methanone

  • 139214-91-8
    139214-91-8

    butyl 2,3,4-trimethoxybenzoate

  • 6395-18-2
    6395-18-2

    methyl 2,3,4-trimethoxybenzoate

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