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5-Methoxy-2,3-dihydroindoline

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CAS:21857-45-4
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Products Intro: Product Name:5-Methoxy-2,3-dihydro-1H-indole
CAS:21857-45-4

5-Methoxy-2,3-dihydroindoline manufacturers

  • 5-Methoxyindoline
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  • $1.10 / 25KG
  • 2025-10-13
  • CAS:21857-45-4
  • Min. Order: 1KG
  • Purity: 99% min
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5-Methoxy-2,3-dihydroindoline Basic information
Product Name:5-Methoxy-2,3-dihydroindoline
Synonyms:1H-INDOLE, 2,3-DIHYDRO-5-METHOXY-;5-METHOXYLINDOLINE;5-METHOXY-2,3-DIHYDRO-1H-INDOLE;5-METHOXY-2,3-DIHYDROINDOLINE;5-Methoxyindoline;5-Methoxy-2,3-dihydro-1H-indoline;5-Methoxyindoline 5-Methoxy-2,3-dihydroindoline in stock Factory; 5-Methoxy-2,3-dihydroindolin
CAS:21857-45-4
MF:C9H11NO
MW:149.19
EINECS:
Product Categories:pharmacetical;Indoline & Oxindole
Mol File:21857-45-4.mol
5-Methoxy-2,3-dihydroindoline Structure
5-Methoxy-2,3-dihydroindoline Chemical Properties
Boiling point 282.6±29.0 °C(Predicted)
density 1.076±0.06 g/cm3(Predicted)
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
form solid
pka6.07±0.20(Predicted)
AppearanceLight yellow to brown Liquid
InChI1S/C9H11NO/c1-11-8-2-3-9-7(6-8)4-5-10-9/h2-3,6,10H,4-5H2,1H3
InChIKeyYYDYAQAVAHKFJO-UHFFFAOYSA-N
SMILESCOc1ccc2NCCc2c1
CAS DataBase Reference21857-45-4(CAS DataBase Reference)
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
WGK Germany WGK 3
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
MSDS Information
5-Methoxy-2,3-dihydroindoline Usage And Synthesis
Synthesis
5-Methoxyindole

1006-94-6

5-Methoxy-2,3-dihydroindoline

21857-45-4

5-Methoxyindole (1.5 g, 10.2 mmol) was dissolved in acetic acid (20 mL) at 25 °C, followed by the addition of sodium cyanoborohydride (0.77 g, 12.2 mmol) in batches. After the reaction lasted for 1 h, the pH of the reaction solution was adjusted to 9-10 with 20% sodium hydroxide solution for neutralization. The reaction mixture was extracted with ethyl acetate (50 mL) and the organic phase was separated and dried over anhydrous sodium sulfate. The dried organic phase was filtered and the filtrate was concentrated by rotary evaporation. Finally, 5-methoxyindoline was purified by column chromatography (eluent: petroleum ether/ethyl acetate, 10:1, v/v) to afford 5-methoxyindoline as a brown solid (1.46 g, 95.9% yield).

References[1] Organic Letters, 2011, vol. 13, # 19, p. 5124 - 5127
[2] Chemical Communications, 2013, vol. 49, # 63, p. 7052 - 7054
[3] Patent: CN105367474, 2016, A. Location in patent: Paragraph 0194; 0195; 0196; 0197
[4] Journal of Medicinal Chemistry, 1997, vol. 40, # 4, p. 479 - 485
[5] Patent: EP1223170, 2002, A1
5-Methoxy-2,3-dihydroindoline Preparation Products And Raw materials
Raw materials5-Methoxyindole-->Sodium carbonate
Preparation ProductsIndolin-5-ol hydrobroMide
Tag:5-Methoxy-2,3-dihydroindoline(21857-45-4) Related Product Information
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