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43200

Sigma-Aldrich

trans-1,3-Diphenyl-2-propen-1-ol

≥98.0% (HPLC)

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Empirical Formula (Hill Notation):
C15H14O
CAS Number:
62668-02-4
Molecular Weight:
210.27
Beilstein:
1951697
MDL number:
MFCD00239426
UNSPSC Code:
12352100
PubChem Substance ID:
57650170
NACRES:
NA.22

Quality Level

100

Assay

≥98.0% (HPLC)

form

solid

mp

55-57 °C

storage temp.

2-8°C

SMILES string

OC(\C=C\c1ccccc1)c2ccccc2

InChI

1S/C15H14O/c16-15(14-9-5-2-6-10-14)12-11-13-7-3-1-4-8-13/h1-12,15-16H/b12-11+

InChI key

ORACYDGVNJGDMI-VAWYXSNFSA-N

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General description

trans-1,3-diphenyl-2-propen-1-ol is an allylic alcohol. It has been reported to exhibit significant in vivo anti-inflammatory activity. Allylic amination of trans-1,3-diphenyl-2-propen-1-ol catalyzed by water-soluble calix[4]resorcinarene sulfonic acid has been reported.

Application

trans-1,3-diphenyl-2-propen-1-ol may be used as a model substrate to investigate the formation of substituted cyclopropanes by SiO2-ZrO2 mixed oxides catalyzed Friedel-Crafts-alkylation followed by trans-hydrogenation.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Direct Nucleophilic SN1-Type Reactions of Alcohols.
Emer E, et al.
European Journal of Organic Chemistry, 4, 647-666 (2011)
Xinqin Liu et al.
International journal of biological sciences, 13(11), 1351-1360 (2017-12-07)
Lead (Pb) is a well-known neurotoxicant and a risk factor for neurologic disorders. The blood brain barrier (BBB) plays an important role in the maintenance of optimal brain function. BBB is a target of Pb, and studies have shown that
Molecular topology as a novel approach for drug discovery.
Galvez J, et al.
Expert Opinion on Drug Delivery, 7(2), 133-153 (2012)
High-Surface-Area SiO2-ZrO2 Mixed Oxides as Catalysts for the Friedel-Crafts-Type Alkylation of Arenes with Alcohols and Tandem Cyclopropanation Reactions.
Kaper H, et al.
ChemCatChem, 4(11), 1813-1818 (2012)

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