Basic information Safety Supplier Related

5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE

Basic information Safety Supplier Related

5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE Basic information

Product Name:
5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE
Synonyms:
  • 5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE
  • 5-CHLORO-3-METHYL-1-PHENYL-4-PYRAZOLECARBOXALDEHYDE
  • 5-CHLORO-3-METHYL-1-PHENYL PYRAZOLE-4-ALDEHYDE
  • 5-CHLORO-3-METHYL-1-PHENYLPYRAZOLE-4-CARBALDEHYDE
  • 5-CHLORO-3-METHYL-1-PHENYLPYRAZOLE-4-CARBOXALDEHYDE
  • 5-CHLORO-4-FORMYL-3-METHYL-1-PHENYLPYRAZOLE
  • OTAVA-BB BB0111070359
  • AKOS BBS-00001388
CAS:
947-95-5
MF:
C11H9ClN2O
MW:
220.65
Product Categories:
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Pyrazoles
  • PyrazolesHeterocyclic Building Blocks
Mol File:
947-95-5.mol
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5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE Chemical Properties

Melting point:
145-148 °C (lit.)
Boiling point:
356.1±37.0 °C(Predicted)
Density 
1.26
refractive index 
1.6000 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
powder to crystal
pka
-3.81±0.10(Predicted)
color 
White to Light yellow
CAS DataBase Reference
947-95-5(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
HazardClass 
IRRITANT
HS Code 
29331990

MSDS

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5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDE Usage And Synthesis

Chemical Properties

light yellow to yellow flakes or needles

Uses

5-Chloro-3-methyl-1-phenyl-4-pyrazolecarboxaldehyde (5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde) may be employed as starting material for the following syntheses:

  • 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde hydrazone
  • N1-((5-chloro-3-methyl-1-phenyl-1H-pyrazol-4-yl)methylene)thiosemicarbazone
  • pyrazole derivatives, which were pharmacologically evaluated for analgesic (tail flick) and anti-inflammatory (based on carrageenan-induced paw edema) activities
  • N′-[(5-chloro-3-methyl-1-phenyl-1H-pyrazol-4- yl)methylene] 2/4-substituted hydrazides

General Description

5-Chloro-3-methyl-1-phenyl-4-pyrazolecarboxaldehyde (5-Chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde) can be synthesized from 3-methyl-1-phenyl-1Hpyrazol-5(4H)-one under Vilsmeier-Haack reaction conditions. Knoevenagel condensation of 5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-carboxaldehyde with ethylcyanoacetate at 0°C has been reported to afford ethyl-2-cyano-3-(5-chloro-3-methyl-1-phenyl-1H-pyrazole-4-yl)propionate. It participates in the synthesis of 2-((5-phenoxy-3-methyl-1-phenyl-1H-pyrazol- 4-yl)methylene)hydrazinecarbothiomide derivatives with a potential anticonvulsant property.

5-CHLORO-3-METHYL-1-PHENYL-1H-PYRAZOLE-4-CARBALDEHYDESupplier

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