4-Bromo-3-nitro pyrazole

4-Bromo-3-nitro pyrazole Suppliers list
Company Name: Shenzhen Nexconn Pharmatechs Ltd
Tel: +86-755-89396905 +86-15013857715
Email: admin@nexconn.com
Products Intro: Product Name:4-BROMO-3-NITRO-1H-PYRAZOLE
CAS:89717-64-6
Purity:98% Package:1KG;10KG;50KG
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Products Intro: Product Name:4-Bromo-3-nitropyrazole
CAS:89717-64-6
Purity:>=97% Package:0.1g;0.25g;1g;5g;10g;25g;100g
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Products Intro: Product Name:4-Bromo-3-nitro-1H-pyrazole
CAS:89717-64-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-18124
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Products Intro: Product Name:4-Bromo-3-nitro pyrazole
CAS:89717-64-6
Purity:98%-99.9% Package:1KG;1USD
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Products Intro: Product Name:4-bromo-5-nitro-1H-pyrazole
CAS:89717-64-6
Purity:0.968 Package:1KG;25KG

4-Bromo-3-nitro pyrazole manufacturers

4-Bromo-3-nitro pyrazole Basic information
Product Name:4-Bromo-3-nitro pyrazole
Synonyms:4-Bromo-3-nitro pyrazole;1H-Pyrazole, 4-broMo-3-nitro-;4-bromo-5-nitro-1H-pyrazole;44-Bromo-3-nitro pyrazole;3-Nitro-4-bromo pyrazole
CAS:89717-64-6
MF:C3H2BrN3O2
MW:191.97
EINECS:
Product Categories:
Mol File:89717-64-6.mol
4-Bromo-3-nitro pyrazole Structure
4-Bromo-3-nitro pyrazole Chemical Properties
Melting point 197-198℃
Boiling point 320.1±22.0 °C(Predicted)
density 2.156
storage temp. Keep in dark place,Sealed in dry,Room Temperature
pka7.03±0.50(Predicted)
AppearanceWhite to off-white Solid
Safety Information
HS Code 2933199090
MSDS Information
4-Bromo-3-nitro pyrazole Usage And Synthesis
Synthesis
3-Nitro-1H-pyrazole

26621-44-3

4-Bromo-3-nitro pyrazole

89717-64-6

General procedure for the synthesis of 4-bromo-3-nitropyrazole from 3-nitro-1H-pyrazole: Water (15 mL) was added to a mixed system containing 3-nitro-1H-pyrazole (48a) (1 g, 8.90 mmol) and N-bromosuccinimide (NBS) (1.73 g, 9.70 mmol) at room temperature and the reaction mixture was stirred continuously overnight. The progress of the reaction was monitored by thin-layer chromatography (TLC) and after confirming that the reaction was complete, the reaction solution was diluted with water and subsequently extracted with ethyl acetate. The organic phase was sequentially washed with saturated sodium chloride solution, dried over anhydrous sodium sulfate, concentrated under reduced pressure, and the solvent was removed by rotary evaporation to afford the target compound 4-bromo-3-nitropyrazole (48b) (1.66 g, 93% yield, white solid). Mass spectrometry (ESI) data: m/z 192 [M + H]+.

References[1] Patent: EP3360878, 2018, A1. Location in patent: Paragraph 0327; 0328
[2] Patent: CN105669558, 2016, A. Location in patent: Paragraph 0057; 0058; 0059; 0060; 0061; 0062; 0063; 0064
[3] Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1984, # 1, p. 63 - 67
[4] Patent: EP1382603, 2004, A1. Location in patent: Page 195; 196
[5] Chemical Biology and Drug Design, 2016, vol. 87, # 4, p. 569 - 574
4-Bromo-3-nitro pyrazole Preparation Products And Raw materials
Raw materials3-Nitro-1H-pyrazole
Preparation Products4-broMo-3-nitro-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole
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