1201-31-6

  • Product Name:2,3,4,5-Tetrafluorobenzoic acid
  • Molecular Formula:C7H2F4O2
  • Purity:99%
  • Molecular Weight:194.085
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Product Details

Factory Sells Best Quality 2,3,4,5-Tetrafluorobenzoic acid 1201-31-6 with USP

  • Molecular Formula:C7H2F4O2
  • Molecular Weight:194.085
  • Appearance/Colour:white to light yellow crystal powder 
  • Melting Point:85-87 °C(lit.) 
  • Boiling Point:239.2 °C at 760 mmHg 
  • PKA:2.53±0.10(Predicted) 
  • Flash Point:98.5 °C 
  • PSA:37.30000 
  • Density:1.633 g/cm3 
  • LogP:1.94120 

2,3,4,5-Tetrafluorobenzoic acid(Cas 1201-31-6) Usage

InChI:InChI=1/C9H12N4O.CHF3O3S/c1-10-3-5-12(7-10)9(14)13-6-4-11(2)8-13;2-1(3,4)8(5,6)7/h3-8H,1-2H3;(H,5,6,7)/q+2;/p-1

1201-31-6 Relevant articles

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Tamborski,C.,Soloski,E.J.

, p. 385 - 391 (1967)

-

Decarboxylation of tetrafluorophthalic acid in NH3-enriched high temperature liquid water

Fu, Jie,Mo, Jing,Zhang, Jing,Lu, Xiuyang

, p. 10 - 15 (2016)

2,3,4,5-Tetrafluorobenzoic acid is an im...

Regiospecific Replacement of Fluorine by Hydrogen in an Aromatic Ring Induced by a Rare Earth Organometallic

Deacon, Glen B.,Forsyth, Craig M.,Sun, Junhui

, p. 1095 - 1098 (1994)

Pentafluorobenzoic acid reacts with YbCp...

Preparation of 2,3,4,5-tetrafluorobenzoic acid

Li, Hua,Wang, Hongkai,Zhao, Ruiju,Liu, Juan,Zhao, Zhengui,Hu, Guoqin,Liang, Zhengyong

, p. 744 - 748 (2010)

2,3,4,5-Tetrafluorobenzoic acid, an impo...

Regioselective ortho-hydrodefluorination of pentafluorobenzoic acid by low-valent nickel complexes

Adonin,Starichenko

, p. 65 - 67 (2000)

2,3,4,5-Tetrafluorobenzoic and 3,4,5-tri...

Elemental fluorine. Part 1. Synthesis of fluoroaromatic compounds

Chambers, Richard D.,Skinner, Christopher J.,Hutchinson, John,Thomson, Julie

, p. 605 - 609 (1996)

Direct fluorination of 4-fluorobenzoic a...

Technological method for preparing 2, 3, 4, 5-tetrachloride phthalic anhydride

-

Paragraph 0039-0044; 0061, (2018/05/01)

The invention relates to an improved tec...

Method for preparing 2,3,4,5-tetrafluoro benzoic acid and 1,2,3,4-tetrafluorobenzene

-

Paragraph 0039; 0040, (2016/11/28)

The present invention discloses a method...

Gold(I)-catalyzed protodecarboxylation of (Hetero)aromatic carboxylic acids

Dupuy, Stéphanie,Nolan, Steven P.

supporting information, p. 14034 - 14038 (2013/11/19)

Readily available, inexpensive and easy ...

1201-31-6 Process route

3,4,5,6-tetrafluorophthalic acid
652-03-9

3,4,5,6-tetrafluorophthalic acid

1,2,3,4-tetrafluorobenzene
551-62-2

1,2,3,4-tetrafluorobenzene

2,3,4,5-tetrafluorobenzoic acid
1201-31-6

2,3,4,5-tetrafluorobenzoic acid

Conditions
Conditions Yield
With ammonium hydroxide; at 190 ℃; for 2h; Temperature; Time; Autoclave; Green chemistry;
86.1%
10.5%
With ammonium hydroxide; at 240 ℃; for 0.666667h; Temperature; Time; Autoclave; Green chemistry;
82%
8.1%
2,4-difluoro-benzoic acid
1583-58-0

2,4-difluoro-benzoic acid

2,3,4,5-tetrafluorobenzoic acid
1201-31-6

2,3,4,5-tetrafluorobenzoic acid

Pentafluorobenzoic acid
602-94-8

Pentafluorobenzoic acid

2,4,5-trifluorobenzoic acid
446-17-3

2,4,5-trifluorobenzoic acid

2,3,4,-trifluorobenzoic acid
61079-72-9

2,3,4,-trifluorobenzoic acid

Conditions
Conditions Yield
With fluorine; In sulfuric acid; Yield given. Yields of byproduct given. Title compound not separated from byproducts;

1201-31-6 Upstream products

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    2,3,4,5-tetrafluorobenzamide

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    carbon dioxide

1201-31-6 Downstream products

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    94695-48-4

    2,3,4,5-tetrafluorobenzoyl chloride

  • 16583-04-3
    16583-04-3

    2-bromo-3,4,5,6-tetrafluorobenzoic acid

  • 122894-73-9
    122894-73-9

    ethyl 2,3,4,5-tetrafluorobenzenecarboxylate