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Sigma-Aldrich

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

≥98.0% (HPLC)

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About This Item

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

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

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Molecular topology as a novel approach for drug discovery.
Galvez J, et al.
Expert Opinion on Drug Delivery, 7(2), 133-153 (2012)
Direct Nucleophilic SN1-Type Reactions of Alcohols.
Emer E, et al.
European Journal of Organic Chemistry, 4, 647-666 (2011)
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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