4-Bromo-1H-pyrazole-3-carboxylic acid

4-Bromo-1H-pyrazole-3-carboxylic acid Suppliers list
Company Name: Jiangsu Aikon Biopharmaceutical R&D co.,Ltd.  Gold
Tel: 025-66028182 17714375163
Email: yftan@aikonchem.com
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Energy Chemical  
Tel: 400-0056266
Email: sales8178@energy-chemical.com
Company Name: Wuhan Chemwish Technology Co., Ltd  
Tel: 86-027-67849912
Email: sales@chemwish.com
Company Name: Pure Chemistry Scientific Inc.  
Tel: 001-857-928-2050 or 1-888-588-9418
Email: sales@chemreagents.com

4-Bromo-1H-pyrazole-3-carboxylic acid manufacturers

4-Bromo-1H-pyrazole-3-carboxylic acid Basic information
Application
Product Name:4-Bromo-1H-pyrazole-3-carboxylic acid
Synonyms:4-Bromopyrazole-3-carboxylic Acid;AKOS B006501;AKOS PAO-1260;4-Bromo-3-carboxy-1H-pyrazole;RARECHEM AL BO 1694;TIMTEC-BB SBB000292;ART-CHEM-BB B006501;CBI-BB ZERO/005392
CAS:13745-17-0
MF:C4H3BrN2O2
MW:190.98
EINECS:
Product Categories:Building Blocks;Pyrazole
Mol File:13745-17-0.mol
4-Bromo-1H-pyrazole-3-carboxylic acid Structure
4-Bromo-1H-pyrazole-3-carboxylic acid Chemical Properties
Melting point 240 °C (decomp)
Boiling point 440.6±30.0 °C(Predicted)
density 2.129±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka2.63±0.10(Predicted)
AppearanceWhite to off-white Solid
InChIInChI=1S/C4H3BrN2O2/c5-2-1-6-7-3(2)4(8)9/h1H,(H,6,7)(H,8,9)
InChIKeyQISOBCMNUJQOJU-UHFFFAOYSA-N
SMILESN1C=C(Br)C(C(O)=O)=N1
Safety Information
HS Code 2933199090
MSDS Information
4-Bromo-1H-pyrazole-3-carboxylic acid Usage And Synthesis
Application4-Bromo-1H-pyrazole-3-carboxylic acid, as a type of pyrazole compound, has been widely used in medicine, pesticides and other fields.
Synthesis
5-Pyrazolecarboxylic acid

1621-91-6

4-BROMO-1H-PYRAZOLE-3-CARBOXYLIC ACID

13745-17-0

The general procedure for the synthesis of 4-bromo-1H-pyrazole-3-carboxylic acid from pyrazole-3-carboxylic acid was as follows: bromine (800 mg, 5.0 mmol) was slowly added to a solution of pyrazole-3-carboxylic acid (500 mg, 4.5 mmol) in acetic acid (20 mL). The reaction mixture was stirred at room temperature for 18 hours. Upon completion of the reaction, it was diluted with water (100 mL) and extracted with ether (3 x 30 mL). All organic phases were combined, washed with water (50 mL), and the solvent was subsequently removed by concentration under reduced pressure to afford the target product 4-bromo-1H-pyrazole-3-carboxylic acid (750 mg, 87% yield) as a light yellow solid. The structure of the product was confirmed by 1H NMR (DMSO-d6, 400 MHz): δ 7.92 (s, 1H).

References[1] Patent: WO2006/32851, 2006, A1. Location in patent: Page/Page column 42
[2] J. Gen. Chem. USSR (Engl. Transl.), 1982, vol. 52, # 11, p. 2291 - 2296
[3] Zhurnal Obshchei Khimii, 1982, vol. 52, # 11, p. 2592 - 2598
[4] Patent: WO2017/100591, 2017, A1. Location in patent: Paragraph 00241
4-Bromo-1H-pyrazole-3-carboxylic acid Preparation Products And Raw materials
Raw materials5-Pyrazolecarboxylic acid-->Acetic acid
Preparation Products1H-Pyrazole-3-carboxylic acid, 4-bromo-1-(1,1-dimethylethyl)-
Tag:4-Bromo-1H-pyrazole-3-carboxylic acid(13745-17-0) Related Product Information
4-Bromo-1 H-pyrazole-3-carboxylic acid hydrazide 4-Bromo-5-pyrazolecarboxylic acid 3-Bromo-1H-pyrazole-4-carboxylicacid Ethyl3-bromo-1H-pyrazole4-carboxylate 5-Pyrazolecarboxylic acid 2,5-Dimethyl-4-bromo-2H-pyrazole-3-carboxylic acid (4-tert-butylbenzyl) ester