328413
(R)-(−)-1-Indanol
99%
Synonym(s):
R(−)-1-Hydroxyindan
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About This Item
Empirical Formula (Hill Notation):
C9H10O
CAS Number:
Molecular Weight:
134.18
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
4350388
Assay:
99%
InChI
1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m1/s1
SMILES string
O[C@@H]1CCc2ccccc12
InChI key
YIAPLDFPUUJILH-SECBINFHSA-N
assay
99%
optical activity
[α]30/D −29°, c = 2 in chloroform
mp
72-73 °C (lit.)
functional group
hydroxyl
Quality Level
Gene Information
human ... UGT2B17(7367), UGT2B7(7364)
Related Categories
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
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Katia Le Barbu-Debus et al.
Physical chemistry chemical physics : PCCP, 20(21), 14635-14646 (2018-05-18)
The influence of flexibility and hydrogen bond formation on the IR absorption and vibrational circular dichroism (VCD) spectrum of a floppy protic molecule, namely, (S)-1-indanol, is studied in both non-polar CCl4 and polar DMSO solvents. The experimental IR absorption and
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
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
Dongmei Zhou et al.
Journal of chromatography. A, 1015(1-2), 73-87 (2003-10-23)
The competitive isotherm data for the enantiomers of 1-indanol were measured on three columns, a microbore column (15 cm x 0.1 cm), a conventional analytical column (15 cm x 0.46 cm), and a semi-preparative column (20 cm x 1.0 cm)
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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