Skip to Content
Merck
All Photos(1)

Documents

563749

Sigma-Aldrich

9-Phenanthrylmagnesium bromide

0.5 M in THF

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C14H9BrMg
CAS Number:
Molecular Weight:
281.43
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

reaction suitability

reaction type: Grignard Reaction

concentration

0.5 M in THF

bp

65 °C (lit.)

density

0.970 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

Br[Mg]c1cc2ccccc2c3ccccc13

InChI

1S/C14H9.BrH.Mg/c1-3-7-13-11(5-1)9-10-12-6-2-4-8-14(12)13;;/h1-9H;1H;/q;;+1/p-1

InChI key

ACMUZKQPXSHTGB-UHFFFAOYSA-M

General description

9-phenanthrylmagnesium bromide is a Grignard reagent. It can be prepared using magnesium turnings and 9-bromophenanthrene under anhydrous condition.

Application

9-Phenanthrylmagnesium bromide can be used as a reagent to prepare:
  • 9-alkyl and 9-arylthiophenanthrenes by reacting with alkyl or aryl thiol compounds.
  • (S)-α-methylbenzyl 1-(9-phenanthryl)-2-naphthoate by treating with (S)- α -methylbenzyl methoxy-2-naphthoate.
  • 1-(9-Phenanthryl)-1-phenylethanol (carbinol) by reacting with acetophenone. The obtained carbinol undergoes dehydration reaction in the presence of acetic acid and sulfuric acid to afford 1-(9-phenanthryl)-1-phenylethene (PPE).

Legal Information

Product of Rieke Metals, Inc.
Rieke is a registered trademark of Rieke Metals, Inc.

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Flam. Liq. 2 - STOT SE 3

Target Organs

Respiratory system

Supplementary Hazards

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

The use of the DPE radical polymerization method for the synthesis of chromophore-labelled polymers and block copolymers
Kos T, et al.
European Polymer Journal, 41(6), 1265-1271 (2005)
Synthesis of 9-alkyl-and 9-arylthiophenanthrenes
Sipila K and Hase T
Synthetic Communications, 27(8), 1391-1393 (1997)
Absolute stereochemistry of 1-(9-phenanthryl)-2-naphthoic acid as determined by CD and X-ray methods
Harada N, et al.
Tetrahedron Asymmetry, 4(8), 1789-1792 (1993)
Novel acyclic nitroxides for nitroxide-mediated polymerization: Kinetic, electron paramagnetic resonance spectroscopic, X-ray diffraction, and molecular modeling investigations
Lagrille O, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 44(6), 1926-1940 (2006)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service