115029-22-6

  • Product Name:2-Fluoro-3- (trifluoromethyl) benzoic acid
  • Molecular Formula:C8H4F4O2
  • Purity:99%
  • Molecular Weight:208.112
Inquiry

Product Details

pd_meltingpoint:126-128 °C(lit.)

Appearance:White to beige crystalline powder

Purity:99%

Factory supply 2-Fluoro-3- (trifluoromethyl) benzoic acid 115029-22-6 with sufficient production capacity

  • Molecular Formula:C8H4F4O2
  • Molecular Weight:208.112
  • Appearance/Colour:White to beige crystalline powder 
  • Vapor Pressure:0.012mmHg at 25°C 
  • Melting Point:126-128 °C(lit.) 
  • Boiling Point:249.6 °C at 760 mmHg 
  • Flash Point:104.7 °C 
  • PSA:37.30000 
  • Density:1.489 g/cm3 
  • LogP:2.54270 

2-FLUORO-3-(TRIFLUOROMETHYL)BENZOIC ACID(Cas 115029-22-6) Usage

InChI:InChI=1/C8H4F4O2/c9-6-4(7(13)14)2-1-3-5(6)8(10,11)12/h1-3H,(H,13,14)/p-1

115029-22-6 Relevant articles

Discovery of Orally Bioavailable Ligand Efficient Quinazolindiones as Potent and Selective Tankyrases Inhibitors

Qin, Donghui,Lin, Xiaojuan,Liu, Zhi,Chen, Yan,Zhang, Zhiliu,Wu, Chengde,Liu, Linlin,Pan, Yan,Laquerre, Sylvie,Emery, John,Fergusson, Jeff,Roland, Kimberly,Keenan, Rick,Oliff, Allen,Kumar, Sanjay,Cheung, Mui,Su, Dai-Shi

, p. 1005 - 1010 (2021)

We report herein the discovery of quinaz...

2-chloro-3-fluoro-4-(trifluoromethyl) benzaldehyde and synthesis method thereof

-

Paragraph 0018-0019; 0030-0031, (2021/04/10)

The invention belongs to the technical f...

P2X7 MODULATORS

-

Paragraph 0284; 0286, (2014/09/29)

The present invention is directed to com...

QUINAZOLINEDIONES AS TANKYRASE INHIBITORS

-

Page/Page column 39, (2014/01/07)

This invention relates to the use of qui...

115029-22-6 Process route

carbon dioxide
124-38-9,18923-20-1

carbon dioxide

1-fluoro-2-trifluoromethylbenzene
392-85-8

1-fluoro-2-trifluoromethylbenzene

2-fluoro-3-(trifluoromethyl)benzoic acid
115029-22-6

2-fluoro-3-(trifluoromethyl)benzoic acid

Conditions
Conditions Yield
1-fluoro-2-trifluoromethylbenzene; With lithium diisopropyl amide; In tetrahydrofuran; at -80 ℃; for 0.666667h; Inert atmosphere;
carbon dioxide; In tetrahydrofuran; for 2h; Inert atmosphere;
With hydrogenchloride; In water; ethyl acetate; Temperature;
90.4%
1-fluoro-2-trifluoromethylbenzene; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 1h; Inert atmosphere;
carbon dioxide; In tetrahydrofuran; at -78 ℃; for 1.83333h;
84%
1-fluoro-2-trifluoromethylbenzene; With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 1h; Inert atmosphere;
carbon dioxide; In tetrahydrofuran; at -78 ℃; for 1.83333h; Inert atmosphere;
84%
2-fluoro-3-(trifluoromethyl)benzoic acid
115029-22-6

2-fluoro-3-(trifluoromethyl)benzoic acid

Conditions
Conditions Yield
With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 4h;

115029-22-6 Upstream products

  • 124-38-9
    124-38-9

    carbon dioxide

  • 392-85-8
    392-85-8

    1-fluoro-2-trifluoromethylbenzene

115029-22-6 Downstream products

  • 680610-54-2
    680610-54-2

    2-fluoro-N-methoxy-N-methyl-3-(trifluoromethyl)benzamide

  • 178748-05-5
    178748-05-5

    methyl 2-fluoro-3-(trifluoromethyl)benzoate

  • 164341-19-9
    164341-19-9

    2-Fluoro-3-trifluoromethylbenzoylguanidine hydrochloride

  • 885328-05-2
    885328-05-2

    tert-butyl 4-(2-fluoro-3-(trifluoromethyl)benzoyl)piperazine-1-carboxylate

Relevant Products