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328413

(R)-(−)-1-Indanol

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

99%

Synonym(s):

R(−)-1-Hydroxyindan

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About This Item

Empirical Formula (Hill Notation):

C₉H₁₀O

CAS Number:

697-64-3

Molecular Weight:

134.18

UNSPSC Code:

12352002

NACRES:

NA.22

PubChem Substance ID:

24859734

MDL number:

MFCD00064164

Beilstein/REAXYS Number:

4350388

Assay:

99%

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Properties

Quality Level

200

assay

99%

optical activity

[α]30/D −29°, c = 2 in chloroform

mp

72-73 °C (lit.)

functional group

hydroxyl

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)

Description

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

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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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

Heterogeneous adsorption of 1-indanol on cellulose tribenzoate and adsorption energy distribution of the two enantiomers.

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

Development of a bioconversion process for production of cis-1S,2R-indandiol from indene by recombinant Escherichia coli constructs.

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

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Global Trade Item Number

SKU	GTIN
328413-1G	04061825932644