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559296

Sigma-Aldrich

2-Phenyl-1,3-propanediol

98%

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About This Item

Linear Formula:
HOCH2CH(C6H5)CH2OH
CAS Number:
1570-95-2
Molecular Weight:
152.19
EC Number:
411-810-2
MDL number:
MFCD00236056
UNSPSC Code:
12352100
PubChem Substance ID:
24879813
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
GHS05

Signal Word

Danger

Hazard Statements

H318

Precautionary Statements

P280 - P305 + P351 + P338

Hazard Classifications

Eye Dam. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
MKCX0594
MKCV8838
MKCW5308
MKCS8399
MKCR9643

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1-Phenyl-1,2-propanedione 99%

Sigma-Aldrich

223034

1-Phenyl-1,2-propanedione

Synthesis, characterization and electrochemistry of phenyl-functionalized diiron propanedithiolate complexes.
Li CG, et al.
Polyhedron, 67, 416-421 (2014)
J Ríha et al.
Veterinarni medicina, 36(2), 65-69 (1991-02-01)
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
Ryoji Mitsui et al.
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
A chemoenzymatic synthesis of both enantiomers of 2-phenyl-3-hydroxypropylcarbamate, a metabolite of felbamate.
Morgan B, et al.
Tetrahedron Asymmetry, 6(7), 1765-1772 (1995)

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