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Methyl 1H-indazole-5-carboxylate

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Products Intro: Product Name:1H-Indazole-5-carboxylic acid methyl ester
CAS:473416-12-5
Purity:98%(Min,HPLC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:methyl 1H-indazole-5-carboxylate
CAS:473416-12-5
Purity:98% Package:10MG;50MG;100MG,1G,5G,10G
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Products Intro: Product Name:5-(1H)INDAZOLE CARBOXYLIC ACID METHYL ESTER
CAS:473416-12-5
Purity:98% Package:1KG;1USD
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Products Intro: Product Name:Methyl 1H-Indazole-5-carboxylate
CAS:473416-12-5
Purity:>97% Package:0.25g;1g;5g;10g;25g;100g;500g
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:Methyl 1H-indazole-5-carboxylate
CAS:473416-12-5
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-12067

Methyl 1H-indazole-5-carboxylate manufacturers

Methyl 1H-indazole-5-carboxylate Basic information
Product Name:Methyl 1H-indazole-5-carboxylate
Synonyms:METHYL 1H-INDAZOLE-5-CARBOXYLATE;5-CARBOXYINDAZOLE METHYL ESTER;5-(1H)INDAZOLE CARBOXYLIC ACID METHYL ESTER;INDAZOLE-5-CARBOXYLIC ACID METHYL ESTER;Methyl indazole-5-carboxylate;1-(1H-indazol-5-yl)propan-1-one;Methyl indazole-5-carboxy...;5-(Methoxycarbonyl)-1H-indazole
CAS:473416-12-5
MF:C9H8N2O2
MW:176.17
EINECS:
Product Categories:Pyrazole series;carboxylic ester
Mol File:473416-12-5.mol
Methyl 1H-indazole-5-carboxylate Structure
Methyl 1H-indazole-5-carboxylate Chemical Properties
Boiling point 345.2±15.0 °C(Predicted)
density 1.324±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form solid
pka12.81±0.40(Predicted)
color Orange
InChIInChI=1S/C9H8N2O2/c1-13-9(12)6-2-3-8-7(4-6)5-10-11-8/h2-5H,1H3,(H,10,11)
InChIKeyLPLOEZPPYOSNEW-UHFFFAOYSA-N
SMILESN1C2=C(C=C(C(OC)=O)C=C2)C=N1
Safety Information
WGK Germany WGK 3
HS Code 2933998090
Storage Class11 - Combustible Solids
MSDS Information
Methyl 1H-indazole-5-carboxylate Usage And Synthesis
Uses5-(1H)INDAZOLE CARBOXYLIC ACID METHYL ESTER is a versatile compound commonly utilized in chemical synthesis as a key building block for the creation of various organic molecules.
Synthesis
Methanol

67-56-1

5-Carboxyindazole hydrochloride

61700-61-6

Methyl 1H-indazole-5-carboxylate

473416-12-5

Concentrated sulfuric acid (0.2 mL) was slowly added to a methanolic (5 mL) suspension of 1H-indazole-5-carboxylic acid (470 mg, 2.9 mmol). The reaction mixture was heated to 70 °C and the reaction was stirred at this temperature overnight. Upon completion of the reaction, the mixture was cooled to room temperature and diluted and neutralized by adding water (10 mL), saturated aqueous sodium bicarbonate (5 mL), and ethyl acetate (30 mL) in that order. The organic and aqueous phases were separated and the aqueous phase was extracted once more with ethyl acetate (30 mL). All organic phases were combined, dried with anhydrous sodium sulfate, filtered and concentrated to dryness under reduced pressure to afford methyl 1H-indazole-5-carboxylate (466 mg, 2.65 mmol, 88% yield) as a light pink to yellow solid. Mass spectrometry analysis showed that the measured value of C9H8N2O2 was (M + H)+ 176.9.

References[1] European Journal of Medicinal Chemistry, 2017, vol. 127, p. 470 - 492
[2] Patent: WO2013/78237, 2013, A1. Location in patent: Page/Page column 81; 82
[3] Patent: WO2016/196776, 2016, A2. Location in patent: Paragraph 00725
[4] Patent: WO2013/96496, 2013, A2. Location in patent: Page/Page column 26
Methyl 1H-indazole-5-carboxylate Preparation Products And Raw materials
Raw materialsMethanol-->Methyl 4-amino-3-methylbenzoate-->METHYL 1-ACETYL-1H-INDAZOLE-5-CARBOXYLATE-->5-Carboxyindazole hydrochloride
Tag:Methyl 1H-indazole-5-carboxylate(473416-12-5) Related Product Information
Indazole 1H-INDAZOLE-4-CARBOXYLIC ACID Indazole-4-boronic acid, hydrochloride 5-Carboxyindazole hydrochloride 1H-INDAZOLE-5-BORONIC ACID 6-INDAZOLYBORONIC ACID 1H-INDAZOLE-5-CARBONITRILE 7-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-1H-INDAZOLE 1H-INDAZOL-7-YL BORONIC ACID (1H-INDAZOL-3-YL)-ACETIC ACID 1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER PROPYL LAURATE Methyl D-(-)-4-hydroxy-phenylglycinate Indazole-3-carboxylic acid 4-(1H)INDAZOLE CARBOXYLIC ACID METHYL ESTER 5-(1H)INDAZOLE CARBOXYLIC ACID METHYL ESTER ETHYL 1H-INDAZOLE-5-CARBOXYLATE 5-Amino-1H-indazole-3-carboxylic acid methyl ester