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328413

(R)-(−)-1-Indanol

Name: (<I>R</I>)-(−)-1-Indanol
Brand: ALDRICH

99%

Sinónimos:

R(−)-1-Hydroxyindan

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About This Item

Fórmula empírica (notación de Hill):

C₉H₁₀O

Número de CAS:

697-64-3

Peso molecular:

134.18

Beilstein/REAXYS Number:

4350388

MDL number:

MFCD00064164

UNSPSC Code:

12352002

PubChem Substance ID:

24859734

NACRES:

NA.22

assay

99%

optical activity

[α]30/D −29°, c = 2 in chloroform

mp

72-73 °C (lit.)

SMILES string

O[C@@H]1CCc2ccccc12

InChI

1S/C9H10O/c10-9-6-5-7-3-1-2-4-8(7)9/h1-4,9-10H,5-6H2/t9-/m1/s1

InChI key

YIAPLDFPUUJILH-SECBINFHSA-N

Gene Information

human ... UGT2B17(7367) , UGT2B7(7364)

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pictograms

GHS07

signalword

Warning

hcodes

H302,H315,H319,H335

pcodes

P261 - P264 - P271 - P301 + P312 - P302 + P352 - P305 + P351 + P338

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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Effect of puckering motion and hydrogen bond formation on the vibrational circular dichroism spectrum of a flexible molecule: the case of (S)-1-indanol.

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

Conformational landscapes and free-jet rotational spectrum of indan-1-ol.

Biagio Velino et al.

Chemphyschem : a European journal of chemical physics and physical chemistry, 7(3), 565-568 (2006-02-14)

Kinetic studies of the inhibition of a human liver 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isozyme by bile acids and anti-inflammatory drugs.

Y Miyabe et al.

Biological & pharmaceutical bulletin, 18(1), 9-12 (1995-01-01)

We have investigated the steady-state kinetics for a cytosolic 3 alpha-hydroxysteroid/dihydrodiol dehydrogenase isozyme of human liver and its inhibition by several bile acids and anti-inflammatory drugs such as indomethacin, flufemanic acid and naproxen. Initial velocity and product inhibition studies performed

Stereospecific oxidation of (R)- and (S)-1-indanol by naphthalene dioxygenase from Pseudomonas sp. strain NCIB 9816-4.

K Lee et al.

Applied and environmental microbiology, 63(5), 2067-2070 (1997-05-01)

A recombinant Escherichia coli strain which expresses naphthalene dioxygenase (NDO) from Pseudomonas sp. strain NCIB 9816-4 oxidized (S)-1-indanol to trans-(1S,3S)-indan-1,3-diol (95.5%) and (R)-3-hydroxy-1-indanone (4.5%). The same cells oxidized (R)-1-indanol to cis-1,3-indandiol (71%), (R)-3-hydroxy-1-indanone (18.2%), and cis-1,2,3-indantriol (10.8%). Purified NDO oxidized

Comparison of the binary equilibrium isotherms of the 1-indanol enantiomers on three high-performance liquid chromatography columns of different sizes.

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)

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