193739
1-Indanol
98%
Synonym(s):
(±)-1-Indanol, (±)-1-Hydroxyindan
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Empirical Formula (Hill Notation):
C9H10O
CAS Number:
Molecular Weight:
134.18
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
228-755-3
Beilstein/REAXYS Number:
2042960
MDL number:
Assay:
98%
Form:
solid
InChI key
YIAPLDFPUUJILH-UHFFFAOYSA-N
InChI
1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2
SMILES string
OC1CCc2ccccc12
assay
98%
form
solid
bp
128 °C/12 mmHg (lit.)
mp
50-54 °C (lit.)
General description
Chiral-sensitive aggregation of 1-indanol has been studied by FTIR spectroscopy. Transfer dehydrogenation of 1-indanol has been investigated over heterogeneous palladium catalyst using cyclohexene as hydrogen acceptor.
signalword
Warning
hcodes
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
Selective transfer dehydrogenation of aromatic alcohols on supported palladium.
Keresszegi C, et al.
New. J. Chem., 25(9), 1163-1167 (2001)
Ticiane C de Souza et al.
Bioprocess and biosystems engineering, 43(12), 2253-2268 (2020-07-30)
In this study, the modulation of enzymatic biocatalysts were developed by the use of lipase B from Candida antarctica covalently immobilized on an eco-friendly support, cashew apple bagasse, activated with 10% glycidol-ethylenediamine-glutaraldehyde (GEG) under different immobilization strategies (5 mM or 100 mM
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service