4-Methoxyindazole-3-carboxylic acid

4-Methoxyindazole-3-carboxylic acid Suppliers list
Company Name: Hangzhou Sage Chemical Co., Ltd.  
Tel: +86057186818502 13588463833
Email: info@sagechem.com
Company Name: Wuhan TCASChem Technology Co., Ltd.  
Tel: 027-86697669 13986148687
Email: sales@tcaschem.com
Company Name: Shanghai Devinchem Ltd  
Tel: 027-65318838 13646286950
Email: sales@devinchem.com
Company Name: Taizhou Tongxin Bio-Tech Co., Ltd  
Tel: 0523-86818997 18652728585
Email: sales@allyrise.com
Company Name: JW & Y Pharmlab Co., Ltd.  
Tel: 021-64340559
Email: xinyu_shi@jwypharmlab.com.cn
4-Methoxyindazole-3-carboxylic acid Basic information
Product Name:4-Methoxyindazole-3-carboxylic acid
Synonyms:1H-Indazole-3-carboxylic acid, 4-methoxy-;4-METHOXYINDAZOLE-3-CARBOXYLIC ACID;4-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID
CAS:865887-02-1
MF:C9H8N2O3
MW:192.17
EINECS:
Product Categories:
Mol File:865887-02-1.mol
4-Methoxyindazole-3-carboxylic acid Structure
4-Methoxyindazole-3-carboxylic acid Chemical Properties
Boiling point 467.6±25.0 °C(Predicted)
density 1.459±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka14.85±0.40(Predicted)
Safety Information
HS Code 2933998090
MSDS Information
4-Methoxyindazole-3-carboxylic acid Usage And Synthesis
Uses4-Methoxy-1H-indazole-3-carboxylic Acid is used in the preparation of tricyclic compounds such as alpha-7 nicotinic acetylcholine receptor ligands for treatment of central nervous system disorders.
Synthesis
4-Methoxy-indoline-2,3-dione

108937-87-7

4-Methoxyindazole-3-carboxylic acid

865887-02-1

The general procedure for the synthesis of 4-methoxy-1H-indazole-3-carboxylic acid from 4-methoxyindoline-2,3-dione was as follows: 4-methoxyindoline-2,3-dione (20.7 mmol) was mixed with 1M sodium hydroxide solution (23 mL) and the reaction mixture was heated to 30-40 °C and maintained at this temperature for 30 minutes. Subsequently, the reaction mixture was cooled to 0 °C and treated with an aqueous solution (5.1 mL) of sodium nitrite (20.7 mmol) and maintained for 20 minutes. This solution was slowly added dropwise to a mixture of concentrated sulfuric acid (2.24 mL) and water (43.3 mL) that had been pre-cooled to 0-5 °C, and the reaction mixture was kept at 0-5 °C for 0.5 hours. Next, a concentrated hydrochloric acid (19.6 mL) solution of tin(II) chloride (50.5 mmol) was added drop by drop and the reaction mixture was kept at 0-5 °C for 1 hour. Upon completion of the reaction, the precipitated solid was separated by filtration and dried to afford 4-methoxy-1H-indazole-3-carboxylic acid as a yellow solid (100% yield).

References[1] Patent: US2007/78147, 2007, A1. Location in patent: Page/Page column 67
4-Methoxyindazole-3-carboxylic acid Preparation Products And Raw materials
Raw materials4-Methoxy-indoline-2,3-dione-->Methyl 4-methoxy-1H-indazole-3-carboxylate-->Sodium hydroxide-->Sodium nitrite
Tag:4-Methoxyindazole-3-carboxylic acid(865887-02-1) Related Product Information
4-Methoxybenzylchloride p-Anisidine 2-Methoxyethanol p-Anisaldehyde 4-Methoxyphenol 4-Methoxybenzoic acid Indazole-3-carboxylic acid (Trifluoromethoxy)benzene Anisole 4-(Trifluoromethoxy)aniline 6-Iodo-4-methoxy-(1H)indazole-3-carboxylic acid 6-Bromo-4-methoxy-3-(1H)indazole carboxylic acid Ethyl 4-methoxy-1H-indazole-3-carboxylate Methyl 4-methoxy-1H-indazole-3-carboxylate 6-Fluoro-4-methoxy-3-(1H)indazole carboxylic acid 6-Chloro-4-methoxy-3-(1H)indazole carboxylic acid 4-Methoxy-6-methyl-3-(1H)indazole carboxylic acid Carboxylic acid