5-Carboxyindazole hydrochloride

5-Carboxyindazole hydrochloride Suppliers list
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Products Intro: Product Name:1H-Indazole-5-carboxylic acid
CAS:61700-61-6
Purity:0.98 Package:25g;34USD|100g;133USD|250g;282USD
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Products Intro: Product Name:1H-Indazole-5-carboxylic acid
CAS:61700-61-6
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:5-Carboxyindazole HCl
CAS:61700-61-6
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Products Intro: Product Name:5-Carboxyindazole hydrochloride
CAS:61700-61-6
Purity:98% Package:1KG;1USD

5-Carboxyindazole hydrochloride manufacturers

5-Carboxyindazole hydrochloride Basic information
Product Name:5-Carboxyindazole hydrochloride
Synonyms:INDAZOLE-5-CARBOXYLIC ACID;5-CARBOXYINDAZOLE HCL;5-CARBOXYINDAZOLE HYDROCHLORIDE;5-INDAZOLECARBOXYLIC ACID;5-(1H)INDAZOLE CARBOXYLIC ACID;1H-Indazole-5-carboxylic acid methyl ester;Indazole-5-carboxylic acid hydrochloride;1-H-indazole-5-carboxyle acid
CAS:61700-61-6
MF:C8H6N2O2
MW:162.15
EINECS:
Product Categories:Building Blocks;Indazole;pharmacetical;Heterocycles series
Mol File:61700-61-6.mol
5-Carboxyindazole hydrochloride Structure
5-Carboxyindazole hydrochloride Chemical Properties
Melting point >250℃
Boiling point 443.7±18.0 °C(Predicted)
density 1.506±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka4.03±0.30(Predicted)
form Spherical Beads
color Yellow to amber
InChI1S/C8H6N2O2/c11-8(12)5-1-2-7-6(3-5)4-9-10-7/h1-4H,(H,9,10)(H,11,12)
InChIKeyMAVGBUDLHOOROM-UHFFFAOYSA-N
SMILESOC(=O)c1ccc2[nH]ncc2c1
CAS DataBase Reference61700-61-6(CAS DataBase Reference)
Safety Information
WGK Germany 3
HazardClass IRRITANT
HS Code 29339980
Storage Class11 - Combustible Solids
MSDS Information
5-Carboxyindazole hydrochloride Usage And Synthesis
Uses1H-Indazole-5-carboxylic Acid is used as a reactant in the synthesis of azabicyclic aryl amides as α7 nicotinic acetylcholine receptor agonists.
Synthesis
Methyl 1H-indazole-5-carboxylate

473416-12-5

5-Carboxyindazole hydrochloride

61700-61-6

General procedure for the synthesis of indazole-5-carboxylic acid hydrochloride from methyl 1H-indazole-5-carboxylate: 1H-indazole-5-carboxylic acid methyl ester (6.5 g, 1.0 eq.) and 200 mL of methanol (MeOH) were added to a stirred 1 L reaction flask, followed by a solution of sodium hydroxide (NaOH, 4.4 g, 3.0 eq.) dissolved in 150 mL of water (H2O). The reaction mixture was heated to reflux for 1 hour. Upon completion of the reaction, the organic solvent was evaporated under reduced pressure. The remaining aqueous phase was washed with ethyl acetate (EtOAc) and then acidified with 3N hydrochloric acid (HCl) to pH=5~6. The precipitate was collected by filtration and washed with deionized water to afford the target product, indazole-5-carboxylic acid hydrochloride, as a yellow solid (6.2 g, 98% yield).

References[1] Patent: WO2013/97773, 2013, A1. Location in patent: Paragraph 0261
[2] Patent: US2012/277224, 2012, A1. Location in patent: Page/Page column 40
[3] Patent: WO2014/66743, 2014, A1. Location in patent: Paragraph 0146
[4] Bioorganic and Medicinal Chemistry, 2006, vol. 14, # 24, p. 8219 - 8248
5-Carboxyindazole hydrochloride Preparation Products And Raw materials
Raw materials1H-INDAZOLE-5-CARBONITRILE-->Methyl 1H-indazole-5-carboxylate-->Sodium hydroxide-->Water-->Methanol
Preparation Products1-BOC-5-INDAZOLECARBOXYLIC ACID
Tag:5-Carboxyindazole hydrochloride(61700-61-6) Related Product Information
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