7-Indazole carboxylic acid methyl ester
- CAS No.
- 952479-65-1
- Chemical Name:
- 7-Indazole carboxylic acid methyl ester
- Synonyms
- METHYL 1H-INDAZOLE-7-CARBOXYLATE;Methyl 2H-indazole-7-carboxylate;7-Indazole carboxylic acid methyl ester;2H-Indazole-7-carboxylic acid methyl ester
- CBNumber:
- CB3666898
- Molecular Formula:
- C9H8N2O2
- Molecular Weight:
- 176.17
- MDL Number:
- MFCD07371608
- MOL File:
- Mol file
- MSDS File:
- SDS
SAFETY
Risk and Safety Statements
| Symbol(GHS) |  GHS07 |
|---|---|
| Signal word | Warning |
| Hazard statements | H315-H319-H335 |
| Precautionary statements | P264-P280-P302+P352-P321-P332+P313-P362-P305+P351+P338-P337+P313-P261-P271-P304+P340-P312-P403+P233-P405-P501 |
7-Indazole carboxylic acid methyl ester price More Price(34)
| Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
|---|---|---|---|---|---|---|---|
| Matrix Scientific | 292154 | Methyl 2H-indazole-7-carboxylate | 952479-65-1 | 250.00mg | $56 | 2026-05-19 | Buy |
| Matrix Scientific | 292154 | Methyl 2H-indazole-7-carboxylate | 952479-65-1 | 1.00g | $110 | 2026-05-19 | Buy |
| Matrix Scientific | 292154 | Methyl 2H-indazole-7-carboxylate | 952479-65-1 | 5.00g | $358 | 2026-05-19 | Buy |
| Synthonix | M51385 | Methyl 2H-indazole-7-carboxylate 95+% | 952479-65-1 | 250mg | $72 | 2026-05-06 | Buy |
| Synthonix | M51385 | Methyl 2H-indazole-7-carboxylate 95+% | 952479-65-1 | 1g | $80 | 2026-05-06 | Buy |
7-Indazole carboxylic acid methyl ester Chemical Properties,Uses,Production
Synthesis
22223-49-0
755752-82-0
General procedure for the synthesis of methyl 1H-indazole-7-carboxylate from methyl 2-amino-3-methylbenzoate: To a solution of methyl 2-amino-3-methylbenzoate (17.5 g, 106 mmol) in chloroform (300 mL) was slowly added acetic anhydride (22.6 mL, 239 mmol, 2.3 eq.), and the temperature of the reaction was controlled to be lower than 40 °C. After addition, the reaction mixture was stirred at room temperature for 1 hour. Subsequently, potassium acetate (3.00 g, 30.6 mmol, 0.3 eq.) and isoamyl nitrite (30.6 mL, 228 mmol, 2.2 eq.) were added and the reaction mixture was heated to reflux for 24 hours. After the reaction was completed, it was cooled to room temperature. The reaction mixture was washed with saturated aqueous sodium bicarbonate, the organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure. Methanol (100 mL) and 6N hydrochloric acid (100 mL) were added to the residue and stirred at room temperature for 18 hours. The solvent was removed under reduced pressure and the residue was ground with ethyl acetate (100 mL). The solid product was collected by filtration, washed with ethyl acetate (20 mL) and dried to give 15.3 g (68% yield) of methyl 1H-indazole-7-carboxylate hydrochloride. The product was characterized by 1H NMR (500 MHz, DMSO-d6) and mass spectrometry (APCI): 1H NMR δ 13.3 (bs, 1H), 8.26 (d, 1H), 8.12 (d, 1H), 8.25 (dd, 1H), 7.27 (t, 1H), 3.97 (s, 3H); MS (APCI) m/z 177 (M++1) .
References
[1] Patent: WO2004/29050, 2004, A1. Location in patent: Page 64
[2] Bioorganic and Medicinal Chemistry, 2015, vol. 23, # 14, p. 3933 - 3937
[3] Journal of Organic Chemistry, 2016, vol. 81, # 15, p. 6855 - 6861
[4] Patent: WO2007/121578, 2007, A1. Location in patent: Page/Page column 29
[5] Patent: WO2008/65508, 2008, A1
7-Indazole carboxylic acid methyl ester Preparation Products And Raw materials
Raw materials
Preparation Products
7-Indazole carboxylic acid methyl ester Suppliers
| Supplier | Tel | Country | ProdList | Advantage | |
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