5-METHOXY-1H-INDAZOLE

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Products Intro: Product Name:5-Methoxy-1H-Indazole
CAS:94444-96-9
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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CAS:94444-96-9
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CAS:94444-96-9
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Products Intro: Product Name:5-Methoxy-1H-indazole
CAS:94444-96-9
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Products Intro: Product Name:5-METHOXY-1H-INDAZOLE
CAS:94444-96-9
Purity:98% HPLC Package:100G;1KG;100KG

5-METHOXY-1H-INDAZOLE manufacturers

  • 5-METHOXY-1H-INDAZOLE
  • 5-METHOXY-1H-INDAZOLE pictures
  • $8.80 / 1KG
  • 2019-07-06
  • CAS:94444-96-9
  • Min. Order: 1KG
  • Purity: 97%-99%
  • Supply Ability: 100kg
5-METHOXY-1H-INDAZOLE Basic information
Product Name:5-METHOXY-1H-INDAZOLE
Synonyms:5-METHOXY-1H-INDAZOLE;5-METHOXYINDAZOLE;5-Methoxy-1H-indazole ,97%;1H-Indazole, 5-methoxy-;2,4-Imidazolidinedione,5-(3-bromophenyl)-7-methyl-;5-Methoxy-1H-indazole?New
CAS:94444-96-9
MF:C8H8N2O
MW:148.16
EINECS:
Product Categories:Indazoles
Mol File:94444-96-9.mol
5-METHOXY-1H-INDAZOLE Structure
5-METHOXY-1H-INDAZOLE Chemical Properties
Melting point 167 °C(Solv: benzene (71-43-2))
Boiling point 312.5±15.0 °C(Predicted)
density 1.244±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka13.61±0.40(Predicted)
AppearanceLight yellow to yellow Solid
InChIInChI=1S/C8H8N2O/c1-11-7-2-3-8-6(4-7)5-9-10-8/h2-5H,1H3,(H,9,10)
InChIKeyGZWWDKIVVTXLFL-UHFFFAOYSA-N
SMILESN1C2=C(C=C(OC)C=C2)C=N1
Safety Information
Risk Statements 22-41
Safety Statements 26-39
HS Code 29339900
MSDS Information
5-METHOXY-1H-INDAZOLE Usage And Synthesis
Chemical PropertiesYellow solid
Synthesis
2-Methyl-4-methoxybenzenamine

102-50-1

5-METHOXY-1H-INDAZOLE

94444-96-9

General procedure for the synthesis of 5-methoxy-1H-indazole using 2-methyl-4-methoxyaniline as starting material: aqueous (8.1 ml) solution of sodium nitrite (3.38 g, 49.0 mmol) was slowly added dropwise to acetic acid (350 ml) solution of 4-methoxy-2-methylaniline (6.69 g, 48.8 mmol) under ice-water bath conditions. The temperature was strictly controlled not to exceed 25°C during the reaction, followed by continuous stirring at room temperature overnight. After completion of the reaction, the reaction mixture was poured into water and extracted with chloroform. The organic layers were combined, washed with saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure and the resulting crude product was purified by silica gel column chromatography (eluent ratio of chloroform/methanol=9/1) to give 5-methoxy-1H-indazole (1.30 g, 18% yield). The product was characterized by 1H-NMR (DMSO-d6) and the chemical shifts δ were 3.76 (3H, s), 6.98 (1H, dd, J=8.8,1.8 Hz), 7.15 (1H, d, J=1.8 Hz), 7.42 (1H, d, J=8.8 Hz), 7.93 (1H, s), and 12.89 (1H, brs).

References[1] Patent: EP1403255, 2004, A1. Location in patent: Page 44
[2] Bulletin of the Chemical Society of Japan, 1985, vol. 58, # 1, p. 309 - 315
[3] Bioorganic and Medicinal Chemistry Letters, 2005, vol. 15, # 23, p. 5293 - 5297
[4] Bioorganic and Medicinal Chemistry Letters, 2001, vol. 11, # 9, p. 1153 - 1156
[5] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 8, p. 2410 - 2414
Tag:5-METHOXY-1H-INDAZOLE(94444-96-9) Related Product Information
5-Benzyloxy-1H-indazole-3-carboxylic acid 5-Methoxy-1H-indazole-3-carboxylic acid ,97% 5-METHOXY-1H-INDAZOLE-3-CARBALDEHYDE, 95+%,5-Methoxy-1H-indazole-3-carboxyaldehyde METHYL 5-METHOXY-1H-INDAZOLE-3-CARBOXYLATE 5-TRIFLUOROMETHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID 5-METHOXY-1H-INDAZOLE-3-CARBONITRILE,3-Cyano-5-methoxy-1H-indazole 3-Cyano-6-methoxy-1H-indazole 3-IODO-6-METHOXY-1H-INDAZOLE 6-Methoxy-1H-indazole-3-carboxyaldehyde 6-Methoxy-1H-indazole 3-Iodo-5,6-dimethoxy-1H-indazole Indazole METHYL 5-BENZYLOXY-1H-INDAZOLE-3-CARBOXYLATE 5,6-DIMETHOXY-1H-INDAZOLE 5,6-DIMETHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID 5,6-DIMETHOXY-1H-INDAZOLE-3-CARBONITRILE 5-METHOXY-1H-INDAZOLE-3-CARBOXYLIC ACID ETHYL ESTER (5-METHOXY-1H-INDAZOL-3-YL)ACETIC ACID

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