1H-Indazole-3-acetic acid, Methyl ester

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Company Name: Coresyn Pharmatech Co., Ltd.
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Products Intro: Product Name:Methyl 2-(1H-indazol-3-yl)acetate
CAS:131666-74-5
Purity:NLT 98% Package:1G;1KG;100KG Remarks:CM28857
Company Name: Zibo Hangyu Biotechnology Development Co., Ltd
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Products Intro: Product Name:Methyl 2-(1H-indazol-3-yl)acetate
CAS:131666-74-5
Purity:99% Package:mg,g,kg
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Products Intro: Product Name:1H-Indazole-3-acetic acid, Methyl ester
CAS:131666-74-5
Purity:0 Package:1g; 5g; 25g; 1kg; 5kg; 25kg Remarks:0
Company Name: Aladdin Scientific
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Products Intro: Product Name:Methyl 2-(1H-indazol-3-yl)acetate
CAS:131666-74-5
Purity:97% Package:$16.9/25mg;$55.9/100mg;$503.9/1g;Bulk package Remarks:97%
Company Name: Compound Net Biotechnology Inc.
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Products Intro: Product Name:methyl 2-(2H-indazol-3-yl)acetate
CAS:131666-74-5
Purity:0.97 Package:5 g; Manufacturer; can be repackaged freely upon request Remarks:100% self-produced and self-developed, not a distributor. Our researchers are graduates of Beijing universities. We have scaling-up capabilities and a base in Shandong.
1H-Indazole-3-acetic acid, Methyl ester Basic information
Product Name:1H-Indazole-3-acetic acid, Methyl ester
Synonyms:1H-Indazole-3-acetic acid, Methyl ester;Methyl 2-(1H-indazol-3-yl)acetate;methyl 1H-Indazole-3-ylacetate;1H-Indazole-3-acetic acid, methyl ester (9CI, ACI);1H-Indazol-3-acetic acid, methyl ester;methyl 2-(2H-indazol-3-yl)acetate
CAS:131666-74-5
MF:C10H10N2O2
MW:190.2
EINECS:
Product Categories:
Mol File:131666-74-5.mol
1H-Indazole-3-acetic acid, Methyl ester Structure
1H-Indazole-3-acetic acid, Methyl ester Chemical Properties
Boiling point 353.3±17.0 °C(Predicted)
density 1.285±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka13.56±0.40(Predicted)
AppearanceWhite to yellow Solid
Safety Information
MSDS Information
1H-Indazole-3-acetic acid, Methyl ester Usage And Synthesis
Synthesis
Methanol

67-56-1

(1H-INDAZOL-3-YL)-ACETIC ACID

26663-42-3

1H-Indazole-3-acetic acid, Methyl ester

131666-74-5

Concentrated sulfuric acid (0.543 g, 5.53 mmol) was slowly added to a stirred solution of indazole-3-acetic acid (4.86 g, 27.5 mmol) in methanol (250 mL). The reaction mixture was refluxed at 68 °C for 16 h, during which the reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the methanol was evaporated to dryness by rotary evaporator. The residual gel was alkalized to pH 7-8 with saturated sodium bicarbonate solution and subsequently extracted with ethyl acetate (3 x 50 mL). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated by rotary evaporator under reduced pressure to give methyl 2-(1H-indazol-3-yl)acetate (4.90 g, 25.7 mmol, 93% yield) as a light brown solid.

References[1] Patent: WO2017/197046, 2017, A1. Location in patent: Page/Page column 328
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 24, p. 7344 - 7350
[3] Tetrahedron, 2012, vol. 68, # 48, p. 10049 - 10058,10
[4] Tetrahedron, 2012, vol. 68, # 48, p. 10049 - 10058
[5] Tetrahedron, 2012, vol. 68, # 49, p. 10180 - 10187
1H-Indazole-3-acetic acid, Methyl ester Preparation Products And Raw materials
Raw materials(1H-INDAZOL-3-YL)-ACETIC ACID-->Methanol
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