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193739

Sigma-Aldrich

1-Indanol

98%

Synonym(s):

(±)-1-Indanol, (±)-1-Hydroxyindan

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About This Item

Empirical Formula (Hill Notation):
C9H10O
CAS Number:
6351-10-6
Molecular Weight:
134.18
Beilstein/REAXYS Number:
2042960
EC Number:
228-755-3
MDL number:
MFCD00003797
UNSPSC Code:
12352100
PubChem Substance ID:
24851607
NACRES:
NA.22

assay

98%

form

solid

bp

128 °C/12 mmHg (lit.)

mp

50-54 °C (lit.)

SMILES string

OC1CCc2ccccc12

InChI

1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2

InChI key

YIAPLDFPUUJILH-UHFFFAOYSA-N

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General description

Chiral-sensitive aggregation of 1-indanol has been studied by FTIR spectroscopy[1]. Transfer dehydrogenation of 1-indanol has been investigated over heterogeneous palladium catalyst using cyclohexene as hydrogen acceptor[2].

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Jonas Altnöder et al.
Physical chemistry chemical physics : PCCP, 15(25), 10167-10180 (2013-05-15)
The aggregation behavior of racemic and enantiopure 1-indanol has been studied by FTIR spectroscopy, resonant ion dip IR spectroscopy, and spontaneous Raman scattering in supersonic jets. This triple experimental approach, augmented by homology to related molecular fragments and dispersion-corrected DFT
Wanda Mączka et al.
Molecules (Basel, Switzerland), 24(23) (2019-12-01)
The main purpose of this publication was to obtain the S-enantiomer of indan-1-ol with high enantiomeric excess and satisfactory yield. In our research, we used carrot callus cultures (Daucuscarota L.), whereby the enzymatic system reduced indan-1-one and oxidized indan-1-ol. During
Selective transfer dehydrogenation of aromatic alcohols on supported palladium.
Keresszegi C, et al.
New. J. Chem., 25(9), 1163-1167 (2001)
J Reddy et al.
Applied microbiology and biotechnology, 51(5), 614-620 (1999-07-03)
Recombinant Escherichia coli cells expressing the toluene dioxygenase (TDO) genes from Pseudomonas putida convert indene to cis-1S,2R-indandiol, a potentially important intermediate for the chemical synthesis of the HIV-1 protease inhibitor, Crixivan. A bioconversion process was developed through optimization of medium
Gustaf Götmar et al.
Analytical chemistry, 76(1), 197-202 (2003-12-31)
The distributions of the adsorption energies (AED) of two enantiomers, (R)-1- indanol and (S)-1-indanol, on a chiral stationary phase were measured and the results are discussed. The chiral phase used is made of cellulose tribenzoate coated on porous silica. The
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