1H-Indazole-3-carboxylic acid, 5-fluoro-, methyl ester

1H-Indazole-3-carboxylic acid, 5-fluoro-, methyl ester - Names and Identifiers

Name	1H-Indazole-3-carboxylicacid, 5-fluoro-, methyl ester
Synonyms	METHYL 5-FLUORO-1H-INDAZOLE-3-CARBOXYLATE Methyl 5-fluoro-1H-indazole-3-carboxylate 5-Fluoro-1H-indazole-3-carboxylicacid methyl ester 5-Fluoro-1H-indazole-3-carboxylic acid methyl ester 1H-Indazole-3-carboxylicacid, 5-fluoro-, methyl ester 1H-Indazole-3-carboxylic acid, 5-fluoro-, methyl ester
CAS	78155-73-4

1H-Indazole-3-carboxylic acid, 5-fluoro-, methyl ester - Physico-chemical Properties

Molecular Formula	C9H7FN2O2
Molar Mass	194.16
Density	1.415
Melting Point	157-161℃
Boling Point	208℃
Flash Point	165℃
pKa	10.83±0.40(Predicted)
Storage Condition	2-8°C

1H-Indazole-3-carboxylic acid, 5-fluoro-, methyl ester - Introduction

5-fluoro, methyl ester is an organic compound with the chemical formula C9H7FN2O2.

Nature:
-Appearance: 5-fluoro-, methyl ester is a colorless to pale yellow solid.
-Melting point: about 86-88 degrees Celsius.
-Boiling point: about 313-315 degrees Celsius.
-Solubility: Good solubility in common organic solvents.

Use:
-Drug intermediates: 5-fluoro-, methyl ester is commonly used as an intermediate in the synthesis of certain medicines. It can be used to synthesize a range of drugs and biologically active compounds.

Preparation Method:
5-fluoro-, methyl ester can be prepared by the following steps:
1. introduction of indazole ring: under the catalysis of sodium hydride or potassium hydride, reaction with alcohol and indazole to generate indazole alcohol.
2. carboxylation reaction: the indazole alcohol reacts with aldehyde acid and sulfurous acid to generate 5-fluorine -1H-indazole -3-carboxylic acid.
3. esterification reaction: 5-fluoro -1H-indazole -3-carboxylic acid is esterified with methanol to form 5-fluoro-methyl ester.

Safety Information:
, 5-fluoro-, methyl ester has low toxicity and irritation to the human body under general operating conditions, but it still needs to be operated based on protection. When in use, wear appropriate protective glasses, protective gloves and laboratory clothing, and ensure that the operating environment is well ventilated. Avoid contact with skin, eyes and mucous membranes, and avoid inhaling their vapors. If exposed or inhaled, rinse immediately with plenty of water and seek medical help. When stored, it should be kept in a closed container, away from fire and oxidizing agents.

Last Update：2024-04-09 15:17:59