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ChemicalBook--->CAS DataBase List--->192944-51-7

192944-51-7

192944-51-7 Structure

192944-51-7 Structure
IdentificationBack Directory
[Name]

ETHYL 1H-INDAZOLE-5-CARBOXYLATE
[CAS]

192944-51-7
[Synonyms]

Ethyl Indazole-5-carboxylate
EthylIndazole-5-carboxylate>
5-(Ethoxycarbonyl)-1H-indazole
ETHYL 1H-INDAZOLE-5-CARBOXYLAT
ETHYL 1H-INDAZOLE-5-CARBOXYLATE
Ethyl1H-indazole-5-carboxylate,95%
Indazole-5-carboxylic Acid Ethyl Ester
1H-INDAZOLE-5-CARBOXYLIC ACID ETHYL ESTER
1H-Indazole-5-carboxylicacid,ethylester(9CI)
[Molecular Formula]

C10H10N2O2
[MDL Number]

MFCD03426220
[MOL File]

192944-51-7.mol
[Molecular Weight]

190.2
Chemical PropertiesBack Directory
[Melting point ]

122-124℃
[Boiling point ]

353.9±15.0 °C(Predicted)
[density ]

1.272±0.06 g/cm3(Predicted)
[storage temp. ]

Inert atmosphere,Room Temperature
[form ]

powder to crystal
[pka]

12.81±0.40(Predicted)
[color ]

White to Yellow to Orange
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P280-P305+P351+P338
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36/37/39
[HS Code ]

29339900
Hazard InformationBack Directory
[Synthesis]

ETHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE

192944-50-6

ETHYL 1H-INDAZOLE-5-CARBOXYLATE

192944-51-7

Ethyl 1-acetyl-1H-indazole-5-carboxylate was used as a raw material, which was dissolved in a mixed solvent consisting of concentrated hydrochloric acid (15 mL), water (15 mL) and ethanol (30 mL), and the reaction was stirred for 4 hours at room temperature. Upon completion of the reaction, the pH of the reaction mixture was adjusted to slightly basic with 25% ammonia. Subsequently, the alkalized mixture was extracted with chloroform. The organic phases were combined and purified by hexane crystallization. After completion of crystallization, the resulting crystals were collected by filtration and dried to give the final ethyl 5-indazolecarboxylate (6.45 g, 48% yield) as a light brown powder.

[References]

[1] Journal of Medicinal Chemistry, 2000, vol. 43, # 1, p. 41 - 58
[2] Patent: US2013/79306, 2013, A1. Location in patent: Paragraph 0286
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