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Merck
CN

56866

(±)-1-Indanol

purum, ≥98.0% (GC)

Synonym(s):

(±)-1-Hydroxyindan

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About This Item

Empirical Formula (Hill Notation):
C9H10O
CAS Number:
Molecular Weight:
134.18
EC Number:
228-755-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
2042960
MDL number:
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grade

purum

assay

≥98.0% (GC)

bp

128 °C/12 mmHg (lit.)

mp

50-53 °C, 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



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Attila Felinger et al.
Journal of chromatography. A, 1005(1-2), 35-49 (2003-08-20)
The inverse method of isotherm determination consists in calculating the numerical values of the coefficients of an isotherm model that give a set of chromatographic profiles in best possible agreement with the set of experimental profiles available. This method was
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