4-INDANOL

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CAS:1641-41-4
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4-INDANOL manufacturers

  • 4-INDANOL
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  • $1.10 / 1g
  • 2025-09-24
  • CAS:1641-41-4
  • Min. Order: 1g
  • Purity: 99.0% min
  • Supply Ability: 100 tons min
  • 4-INDANOL
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  • $0.00 / 25KG
  • 2025-07-25
  • CAS:1641-41-4
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  • Purity: 98.0%
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  • 4-INDANOL
  • 4-INDANOL pictures
  • $0.10 / 1KG
  • 2024-08-05
  • CAS:1641-41-4
  • Min. Order: 1KG
  • Purity: 98.0%
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4-INDANOL Basic information
Product Name:4-INDANOL
Synonyms:4-INDANOL;1H-Inden-4-ol, 2,3-dihydro-;indan-4-ol;2,3-Dihydro-1H-inden-4-ol;4-Hydroxyindane;4-Hydroxyhydrindene;4-Hydroxyindan;NSC 64460
CAS:1641-41-4
MF:C9H10O
MW:134.18
EINECS:216-691-9
Product Categories:
Mol File:1641-41-4.mol
4-INDANOL Structure
4-INDANOL Chemical Properties
Melting point 47-51 °C
Boiling point 245 °C
density 1.147±0.06 g/cm3(Predicted)
storage temp. 2-8°C
form liquid
pkapK1:10.32 (25°C)
color Light brown
InChIInChI=1S/C9H10O/c10-9-6-2-4-7-3-1-5-8(7)9/h2,4,6,10H,1,3,5H2
InChIKeyDPHNJPUOMLRELT-UHFFFAOYSA-N
SMILESC1C2=C(C(O)=CC=C2)CC1
Safety Information
RIDADR 2811
HazardClass 6.1
PackingGroup 
HS Code 2906290090
MSDS Information
4-INDANOL Usage And Synthesis
Synthesis
4-Hydroxyindan-1-one

40731-98-4

4-INDANOL

1641-41-4

The general procedure for the synthesis of 2,3-dihydro-1H-4-indanol from 4-hydroxy-1-indanone was as follows: NaCNBH3 (6.4 g, 101.1 mmol) was added to a mixture of 4-hydroxy-1-indanone (5.0 g, 33.7 mmol) and zinc iodide (32.3 g, 101.1 mmol) in ethylene chloride (100 mL). The reaction mixture was stirred under reflux conditions for 2 hours. After completion of the reaction, it was filtered through silica gel (SiO2) while hot and eluted with dichloroethane. The filtrate was collected and concentrated under reduced pressure. The residue was dissolved in ether and filtered to remove the resulting white precipitate. The filtrate was collected again, concentrated in vacuum and finally purified by fast column chromatography to afford the target product 2,3-dihydro-1H-4-indanol (3 g, yield: 66%). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.02 (m, 1H), 6.80 (d, J = 5.2 Hz, 1H), 6.61 (m, 1H), 2.91 (m, 4H), 2.05 (m, 2H).

References[1] Patent: US2011/152246, 2011, A1. Location in patent: Page/Page column 118-119
[2] Patent: CN108997163, 2018, A. Location in patent: Paragraph 0094; 0098; 0099
[3] Bioorganic and Medicinal Chemistry Letters, 2007, vol. 17, # 16, p. 4625 - 4629
[4] Patent: US2003/207916, 2003, A1
[5] Patent: US2004/209936, 2004, A1
Tag:4-INDANOL(1641-41-4) Related Product Information
[1S,(+)]-1-Indanol 3-(4-Hydroxyphenyl)-1,1,3-trimethyl-5-indanol CARBENICILLIN INDANYL SODIUM 1-(1-Butyl-4-piperidyl)-2-methyl-2-phenyl-1-indanol (1S,2S)-1-Amino-2-indanol (1S,2R)-(-)-cis-1-Amino-2-indanol 2-BROMO-1-INDANOL (1R,2R)-N-BOC-1-AMINO-2-INDANOL (1R,2R)-1-Amino-2-indanol,(1R,2R)-(-)-TRANS-1-AMINO-2-INDANOL 1-METHOXY-2-INDANOL 98+%,1-METHOXY-2-INDANOL (±)-1-Hydroxyindan, (±)-1-Indanol,1-INDANOL,(+/-)-1-INDANOL (1R, 25) - (+) CIS-1-AMINO-2-INDANOL,(1R,2S)-(+)-1-AMINO-2-INDANOL,(1R,2S)-1-AMINO-2-INDANOL,(1R,2S)-CIS-1-AMINO-2-INDANOL,(1R,2S)-(+)-CIS-1-AMINO-2-INDANOL 5-INDANOL 99% 2-INDANOL 99%,2-INDANOL 3,3-DIMETHYL-1-INDANOL 1,1-Dimethyl-4-indanol 5-Bromo-2,3-dihydro-1H-inden-1-ol (1R,2S)-N-BOC-1-AMINO-2-INDANOL

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