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Key Documents

559296

Sigma-Aldrich

2-Phenyl-1,3-propanediol

98%

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About This Item

Linear Formula:
HOCH2CH(C6H5)CH2OH
CAS Number:
Molecular Weight:
152.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

98%

mp

53-56 °C (lit.)

functional group

hydroxyl
phenyl

SMILES string

OCC(CO)c1ccccc1

InChI

1S/C9H12O2/c10-6-9(7-11)8-4-2-1-3-5-8/h1-5,9-11H,6-7H2

InChI key

BPBDZXFJDMJLIB-UHFFFAOYSA-N

Application

2-Phenyl-1,3-propanediol may be used to synthesize enantiomers of 2-phenyl-3-hydroxypropylcarbamate, via a chemoenzymatic method. It may also be employed in the preparation of 2-phenyl-1,3-propanedithiol.

pictograms

Corrosion

signalword

Danger

hcodes

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable


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In practical farming conditions of an agricultural enterprise situated in South-East Moravia, the repellents N,N'-diethyl-m-toluamide and 2-phenyl propanediol 1,3 were tested after their application to grazing first-calves of the Bohemian Pied breed. The experiment was conducted in July and August
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Bioscience, biotechnology, and biochemistry, 71(8), 1858-1864 (2007-08-11)
Bacillus cereus 809A and Burkholderia sp. 711C were isolated from soil. These strains demonstrate hydrolysis activity towards prochiral 2-phenyl-1,3-propanediol diacetate and accumulated the corresponding chiral monoacetates into the reaction mixture. When 2-phenyl 1,3-propanediol diacetate was used as a substrate, the
Synthesis, characterization and electrochemistry of phenyl-functionalized diiron propanedithiolate complexes.
Li CG, et al.
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A chemoenzymatic synthesis of both enantiomers of 2-phenyl-3-hydroxypropylcarbamate, a metabolite of felbamate.
Morgan B, et al.
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