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3-chloro-1H-pyrazole

Product Name
3-chloro-1H-pyrazole
CAS No.
14339-33-4
Chemical Name
3-chloro-1H-pyrazole
Synonyms
EOS-61387;3-Chloroyrazole;3-Chloropyrazole;5-Chloropyrazole;3-chloro-1H-pyrazole;1H-Pyrazole, 3-chloro-
CBNumber
CB42593960
Molecular Formula
C3H3ClN2
Formula Weight
102.52
MOL File
14339-33-4.mol
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3-chloro-1H-pyrazole Property

Melting point:
40 °C
Boiling point:
250.9±13.0 °C(Predicted)
Density 
1.405±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder
pka
11.04±0.10(Predicted)
color 
White
InChI
InChI=1S/C3H3ClN2/c4-3-1-2-5-6-3/h1-2H,(H,5,6)
InChIKey
IJPFBRONCJOTTA-UHFFFAOYSA-N
SMILES
N1C=CC(Cl)=N1
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Safety

HS Code 
2933992000
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P312Call a POISON CENTER or doctor/physician if you feel unwell.

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N-Bromosuccinimide Price

Apolloscientific
Product number
OR183405
Product name
3-Chloro-1H-pyrazole
Purity
95%
Packaging
1g
Price
$56
Updated
2021/12/16
SynQuest Laboratories
Product number
3H31-5-1H
Product name
3-Chloro-1H-pyrazole
Purity
95%
Packaging
1g
Price
$61
Updated
2021/12/16
AK Scientific
Product number
7033AA
Product name
3-Chloro-1H-pyrazole
Packaging
250mg
Price
$89
Updated
2021/12/16
Apolloscientific
Product number
OR183405
Product name
3-Chloro-1H-pyrazole
Purity
95%
Packaging
5g
Price
$182
Updated
2021/12/16
SynQuest Laboratories
Product number
3H31-5-1H
Product name
3-Chloro-1H-pyrazole
Purity
95%
Packaging
5G
Price
$200
Updated
2021/12/16
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3-chloro-1H-pyrazole Chemical Properties,Usage,Production

Uses

5-Chloro-1h-pyrazole is used in preparation of aminoquinazolines as P2X3 inhibitors.

Synthesis

1820-80-0

14339-33-4

General procedure for the synthesis of 3-chloro-1H-pyrazole from 3-aminopyrazole: Concentrated hydrochloric acid (20 mL) was slowly added to a solution of acetonitrile (600 mL) containing 1H-pyrazol-3-amine (20.0 g, 241 mmol), followed by the addition of copper(II) chloride (65.0 g, 481 mmol) at 0 °C. The reaction mixture was stirred at 0 °C for 30 min followed by dropwise addition of isoamyl nitrite (56.4 g, 481 mmol). The reaction mixture was continued to be stirred at room temperature for 2 days. After completion of the reaction, the reaction was quenched with 10% aqueous ammonia solution (1 L). The aqueous phase was extracted with ethyl acetate (5 x 500 mL) and the combined organic phases were washed with saturated brine, dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate=20:1) to afford the target product 3-chloro-1H-pyrazole (10.3 g, 42% yield) as a green oil.1H NMR (400 MHz, CDCl3): δ 12.84 (br s, 1H), 7.62 (s, 1H), 6.29 (s, 1H).

References

[1] Patent: WO2018/85247, 2018, A1. Location in patent: Paragraph 00296; 00297

3-chloro-1H-pyrazole Preparation Products And Raw materials

Raw materials

Preparation Products

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3-chloro-1H-pyrazole Suppliers

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14339-33-4, 3-chloro-1H-pyrazoleRelated Search:


  • 3-chloro-1H-pyrazole
  • 1H-Pyrazole, 3-chloro-
  • 5-Chloropyrazole
  • 3-Chloropyrazole
  • EOS-61387
  • 3-Chloroyrazole
  • 14339-33-4