9-Bromophenanthrene

9-Bromophenanthrene
  • CAS No.:573-17-1
Other grades of this product :
9-Bromophenanthrene Basic information
Product Name:9-Bromophenanthrene
Synonyms:9-BROMOPHENANTHRENE;9-Bromophenathrene;9-Bromophenanthrene,95%;9-Bromophenanthrene,97%;Phenanthrene, 9-bromo-;9-Bromoanth raceme 96%;9-Bromophenanthrene,96%;9-BroMophenanthrene, 96% 10GR
CAS:573-17-1
MF:C14H9Br
MW:257.13
EINECS:209-351-6
Product Categories:blocks;Bromides;Miscellaneous;Aryl;C13 to C37+;Halogenated Hydrocarbons;Aromatic Compounds;bc0001
Mol File:573-17-1.mol
9-Bromophenanthrene Chemical Properties
Melting point 60-64 °C (lit.)
Boiling point 180-190 °C/2 mmHg (lit.)
density 1.4251 (rough estimate)
refractive index 1.6404 (estimate)
Fp >230 °F
storage temp. Sealed in dry,Room Temperature
solubility chloroform: 50 mg/mL, clear
form Powder
color Light yellow
BRN 1869927
InChIKeyRSQXKVWKJVUZDG-UHFFFAOYSA-N
CAS DataBase Reference573-17-1(CAS DataBase Reference)
NIST Chemistry ReferencePhenanthrene, 9-bromo-(573-17-1)
Safety Information
Hazard Codes Xi,Xn
Risk Statements 20/21/22-36/37/38
Safety Statements 22-24/25-36-26
WGK Germany 3
RTECS SF7197000
8
Hazard Note Irritant
HS Code 29036990
MSDS Information
ProviderLanguage
9-Bromophenanthrene English
SigmaAldrich English
ACROS English
ALFA English
9-Bromophenanthrene Usage And Synthesis
Chemical Propertieslight yellow powder
Chemical PropertiesSoluble in toluene, and chloroform (50 mg/ml)
Uses9-Bromophenanthrene is used as halogenated building block. Isotope labelled 9-Bromophenanthrene (B687200), a halogenated polycyclic aromatic hydrocarbon that has been seen to have a room temperature phosphorescence that can be induced by β-cyclodextrin (β-CD) in the presence of cyclohexane; however, trace Fe(III) causes a decrease of the RTP emission.
Preparation9-Bromophenanthrene (90-94%) is produced by adding bromine to a refluxing solution of phenanthrene in carbon tetrachloride. This is the starting-point of 9-substituted phenanthrenes, e.g, when heated with cuprous cyanide at 260℃, 9-bromophenanthrene forms the corresponding cyano-compound; this may be hydrolysed to phenanthrene-9-carboxylic acid. Phenanthrene undergoes the Friedel-Crafts reaction mainly in the 3-, and to a small extent, in the 2-position. It is chloromethylated in the 9-position. When nitrated, phenanthrene gives a mixture of three mononitro-derivatives, the 3-isomer predominating. Sulphonation of phenanthrene gives a mixture of 1-, 2-, 3- and 9-phenanthrenesulphonic acids, and the ratio of these isomers depends on the temperature.

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