3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde

3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Suppliers list
Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
Tel: 4006356688 18621169109
Email: market03@meryer.com
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
Email: sales@chemreagents.com
Company Name: ZEROSCHEM.CO.,LTD.  
Tel: 10-61256048 13810278579;
Email: sales@zeroschem.com
Company Name: Bide Pharmatech Ltd.  
Tel: 400-164-7117 18317119277
Email: product02@bidepharm.com
Company Name: Modachem Shanghai Co., Ltd  
Tel: +86 (0)21 51320687 51371369 1744605818
Email:
3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Basic information
Uses
Product Name:3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde
Synonyms:3-(Trifluoromethyl)-1H-pyrazole-4-carboxaldehyde;4-Formyl-3-(trifluoromethyl)-1H-pyrazole;1H-Pyrazole-4-carboxaldehyde, 3-(trifluoromethyl)-;5-(trifluoromethyl)-1H-pyrazole-4-carbaldehyde;3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde
CAS:1001020-14-9
MF:C5H3F3N2O
MW:164.09
EINECS:
Product Categories:Pyrazoles & Triazoles;Aldehydes;Pyrazoles & Triazoles
Mol File:Mol File
3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Structure
3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Chemical Properties
Boiling point 285.7±40.0 °C(Predicted)
density 1.545±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka8.21±0.50(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933199090
MSDS Information
3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Usage And Synthesis
Uses3-(trifluoromethyl)pyrazole-4-carboxaldehyde is an aldehyde organic compound that can be used as an organic intermediate.
Synthesis
3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol

1001020-13-8

3-TRIFLUOROMETHYL-1H-PYRAZOLE-4-CARBALDEHYDE

1001020-14-9

3-(Trifluoromethyl)-1H-pyrazol-4-ylmethanol (54.00 g, 0.325 mol) was used as a raw material and suspended in toluene (2 L). Manganese dioxide (113.00 g, 1.30 mol) and 4molecular sieve powder (54.00 g) were added to the suspension. The reaction mixture was stirred at reflux for 5.5 hours under nitrogen protection, assembled with a Dean-Stark splitter. Upon completion of the reaction, the reaction mixture was filtered while hot, the filter cake was collected and cooled to room temperature. The filter cake was washed with a 1:1 mixture of dichloromethane and methanol (3 x 500 mL). All the filtrates were combined and the solvent was removed by concentration under reduced pressure to afford the target product 3-(trifluoromethyl)pyrazole-4-carbaldehyde (54.00 g, 0.329 mol, 100% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6): δ 8.72 (s, 1H), 9.91 (s, 1H).

References[1] Patent: US2009/131455, 2009, A1. Location in patent: Page/Page column 8
[2] Patent: WO2008/3452, 2008, A1. Location in patent: Page/Page column 53
3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde Preparation Products And Raw materials
Raw materials3-(trifluoroMethyl)-1H-Pyrazole-4-Methanol-->Manganese dioxide-->Molecular sieve 3A-->Toluene
Tag:3-Trifluoromethyl-1H-pyrazole-4-carbaldehyde(1001020-14-9) Related Product Information
3-Trifluoromethyl-2-formylpyridine 1-Methyl-1H-pyrazole-4-boronic acid 3-(Trifluoromethyl)-6,7,8,9-tetrahydro-5H-carbazole methyl 3-trifluoro-2-pyridinecarboxylate 3-(Trifluoromethyl)pyrazole Ethyl 3-(trifluoromethyl)pyrazole-4-carboxylate