Basic information Uses Safety Supplier Related

4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID

Basic information Uses Safety Supplier Related

4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID Basic information

Product Name:
4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID
Synonyms:
  • 4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID
  • 4-Iodo-1-methylpyrazole-5-carboxylic Acid
  • 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid(SALTDATA: FREE)
  • 4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid 98%
  • 5-Carboxy-4-iodo-1-methyl-1H-pyrazole, 4-Iodo-2-methyl-2H-pyrazole-3-carboxylic acid
  • 4-iodo-2-methylpyrazole-3-carboxylic acid
  • 4-Iodo-1-methyl-1H-pyrazole-5-carboxylicacid98%
  • 4-Iodo-1-methylpyrazole-5-carboxylicAcid>
CAS:
75092-30-7
MF:
C5H5IN2O2
MW:
252.01
Product Categories:
  • HFC00039
Mol File:
75092-30-7.mol
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4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID Chemical Properties

Melting point:
242°C(lit.)
Boiling point:
362.2±27.0 °C(Predicted)
Density 
2.26±0.1 g/cm3(Predicted)
storage temp. 
2-8°C(protect from light)
form 
powder to crystal
pka
1.76±0.37(Predicted)
color 
White to Almost white
CAS DataBase Reference
75092-30-7
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Safety Information

HazardClass 
IRRITANT
HS Code 
2933199090
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4-IODO-1-METHYL-1H-PYRAZOLE-5-CARBOXYLIC ACID Usage And Synthesis

Uses

4-Iodo-1-methyl-1H-pyrazole-5-carboxylic acid is a carboxylic acid derivative that can be used as a pharmaceutical intermediate.

Synthesis

1354705-42-2

75092-30-7

General procedure for the synthesis of 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid from ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate: to a stirred solution of ethyl 4-iodo-1-methyl-1H-pyrazole-5-carboxylate (700 mg, 2.5 mmol) in a solvent mixture of 15 mL MeOH/H2O/THF (v/v/v = 1:1:1) Lithium hydroxide monohydrate (1.05 g, 25 mmol) was added. After addition, the reaction solution was stirred at 25°C for 2 hours. After the completion of the reaction, the mixture was concentrated under reduced pressure and the pH was adjusted to 4 with 1N HCl. The aqueous phase was extracted with EtOAc, and the organic layers were combined, washed with saturated brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure to obtain the crude 4-iodo-1-methyl-1H-pyrazole-5-carboxylic acid (623.0 mg, crude yield 98%), which was used directly in the next step without further purification. The crude product was directly used in the next step without further purification.

References

[1] Patent: US2014/200215, 2014, A1. Location in patent: Paragraph 1002; 1006

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