1H-INDAZOLE-7-CARBOXYLIC ACID
- CAS No.
- 755752-82-0
- Chemical Name:
- 1H-INDAZOLE-7-CARBOXYLIC ACID
- Synonyms
- Niraparib Intermediate5;7-INDAZOLE CARBOXYLLIC ACID;Methyl indazole-7-carboxy...;Methyl indazole-7-carboxylate;Methyl 1H-Indazole-7-carboxyate;7-(Methoxycarbonyl)-1H-indazole;1H-Indazole-7-carboxylic acid methyl ester;7-(1H)Indazole carboxylic acid Methyl ester;1H-Indazole-7-carboxylic acid methyl ester
- CBNumber:
- CB2197276
- Molecular Formula:
- C9H8N2O2
- Molecular Weight:
- 176.17
- MDL Number:
- MFCD07371608
- MOL File:
- 755752-82-0.mol
Boiling point | 345.2±15.0 °C(Predicted) |
---|---|
Density | 1.324 |
storage temp. | Sealed in dry,Room Temperature |
form | solid |
pka | 11.93±0.40(Predicted) |
Appearance | Light yellow to yellow Solid |
InChI | InChI=1S/C9H8N2O2/c1-13-9(12)7-4-2-3-6-5-10-11-8(6)7/h2-5H,1H3,(H,10,11) |
InChIKey | GEWJEKADAXWFPY-UHFFFAOYSA-N |
SMILES | N1C2=C(C=CC=C2C(OC)=O)C=N1 |
CAS DataBase Reference | 755752-82-0 |
UNSPSC Code | 12352200 |
SAFETY
Risk and Safety Statements
Symbol(GHS) | ![]() GHS07 |
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Signal word | Warning | |||||||||
Hazard statements | H315-H319-H335 | |||||||||
Precautionary statements | P261-P280a-P304+P340-P305+P351+P338-P405-P501a | |||||||||
WGK Germany | 3 | |||||||||
HS Code | 2933998090 | |||||||||
NFPA 704 |
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1H-INDAZOLE-7-CARBOXYLIC ACID price More Price(22)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich | SYX00166 | 1H-Indazole-7-carboxylic acid methyl ester Aldrich | 755752-82-0 | 1g | $185 | 2025-07-31 | Buy |
TRC | M313528 | Methylindazole-7-carboxylate | 755752-82-0 | 100mg | $45 | 2021-12-16 | Buy |
TRC | M313528 | Methylindazole-7-carboxylate | 755752-82-0 | 250mg | $55 | 2021-12-16 | Buy |
TRC | M313528 | Methylindazole-7-carboxylate | 755752-82-0 | 500mg | $65 | 2021-12-16 | Buy |
Apolloscientific | OR30717 | Methyl1H-indazole-7-carboxylate 98% | 755752-82-0 | 5g | $61 | 2021-12-16 | Buy |
1H-INDAZOLE-7-CARBOXYLIC ACID 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. The reaction mixture was stirred for 1 hour at room temperature. The reaction mixture was stirred at room temperature for 1 hour and then potassium acetate (3.00 g, 30.6 mmol, 0.3 eq.) and isoamyl nitrite (30.6 mL, 228 mmol, 2.2 eq.) were added sequentially. The reaction mixture was heated to reflux for 24 hours and subsequently 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 the mixture was stirred at room temperature for 18 hours. The volatiles were removed under reduced pressure and the residue was ground with ethyl acetate (100 mL). The solid product was separated by filtration, washed with ethyl acetate (20 mL) and dried to give 15.3 g (68% yield) of methyl 1H-indazole-7-carboxylate hydrochloride. Product characterization data: 1H NMR (500 MHz, DMSO-d6) δ; 13.3 (broad peak, 1H), 8.26 (double peak, 1H), 8.12 (double peak, 1H), 8.25 (double-double peak, 1H), 7.27 (triple peak, 1H), 3.97 (single peak, 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
1H-INDAZOLE-7-CARBOXYLIC ACID Preparation Products And Raw materials
Raw materials
Preparation Products
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
Capot Chemical Co.,Ltd. | +8613336195806 | sales@capot.com | China | 29734 | 60 |
Beijing Cooperate Pharmaceutical Co.,Ltd | 010-60279497 | sales01@cooperate-pharm.com | CHINA | 1803 | 55 |
ATK CHEMICAL COMPANY LIMITED | +undefined-21-51877795 | ivan@atkchemical.com | China | 33024 | 60 |
career henan chemical co | +86-0371-86658258 +8613203830695 | sales@coreychem.com | China | 29855 | 58 |
Shanghai Arbor Chemical Co., Ltd. | 021-60451682 | act@arborchemical.com | CHINA | 904 | 58 |
Jinan Carbotang Biotech Co.,Ltd. | +8615866703830 | figo.gao@foxmail.com | China | 8497 | 58 |
Nanjing Dolon Biotechnology Co.,Ltd. | 18905173768 | 52513593@qq.com | CHINA | 2972 | 58 |
Accela ChemBio Inc. | +1-858-6993322 | info@accelachem.com | United States | 21193 | 58 |
Alchem Pharmtech,Inc. | 8485655694 | sales@alchempharmtech.com | United States | 63687 | 58 |
CONIER CHEM AND PHARMA LIMITED | +8618523575427 | sales@conier.com | China | 49975 | 58 |
View Lastest Price from 1H-INDAZOLE-7-CARBOXYLIC ACID manufacturers
Image | Update time | Product | Price | Min. Order | Purity | Supply Ability | Manufacturer | |
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2025-04-04 | 1H-INDAZOLE-7-CARBOXYLIC ACID
755752-82-0
|
US $0.00-0.00 / KG | 1KG | 98% | 1ton | Henan Aochuang Chemical Co.,Ltd.
|
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2024-11-26 | Methyl 1H-Indazole-7-carboxyate
755752-82-0
|
US $0.00-0.00 / kg | 1kg | 98% | 1 ton | Nanjing Fred Technology Co., Ltd | |
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2019-07-06 | 1H-INDAZOLE-7-CARBOXYLIC ACID
755752-82-0
|
US $500.00 / KG | 1KG | 98% | 1ton | Career Henan Chemical Co |
-
- 1H-INDAZOLE-7-CARBOXYLIC ACID
755752-82-0
- US $0.00-0.00 / KG
- 98%
- Henan Aochuang Chemical Co.,Ltd.
-
- Methyl 1H-Indazole-7-carboxyate
755752-82-0
- US $0.00-0.00 / kg
- 98%
- Nanjing Fred Technology Co., Ltd
-
- 1H-INDAZOLE-7-CARBOXYLIC ACID
755752-82-0
- US $500.00 / KG
- 98%
- Career Henan Chemical Co
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