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230-07-9

230-07-9 Structure

230-07-9 Structure
IdentificationBack Directory
[Name]

4,7-PHENANTHROLINE
[CAS]

230-07-9
[Synonyms]

AKOS 92616
P-PHENANTHROLINE
AKOS BBS-00001338
4,7-PHENANTHROLINE
Pseudophenanthroline
OTAVA-BB BB7110952551
1,8-Diazaphenanthrene
P-PHENANTHROLINE (4,7)
4,7-Phenanthroline 98%
4,7-Phenanthroline (7CI, 8CI, 9CI, ACI)
4,7-PHENANTHROLINE, 98%4,7-PHENANTHROLINE, 98%4,7-PHENANTHROLINE, 98%4,7-PHENANTHROLINE, 98%
[Molecular Formula]

C12H8N2
[MDL Number]

MFCD00004987
[MOL File]

230-07-9.mol
[Molecular Weight]

180.21
Chemical PropertiesBack Directory
[Melting point ]

172-174 °C(lit.)
[Boiling point ]

303.03°C (rough estimate)
[density ]

1.1836 (rough estimate)
[refractive index ]

1.5200 (estimate)
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Crystalline Powder
[pka]

4.30±0.10(Predicted)
[color ]

White to beige
[Water Solubility ]

1.442g/L(temperature not stated)
[InChIKey]

DATYUTWESAKQQM-UHFFFAOYSA-N
Safety DataBack Directory
[Hazard Codes ]

Xn
[Risk Statements ]

22-41-36/37/38
[Safety Statements ]

26-39-36
[WGK Germany ]

3
[HS Code ]

29339900
Hazard InformationBack Directory
[Uses]

4,7-Phenanthroline was used in preparation of:
  • cyclic tetranuclear half-sandwich ruthenium(II) complexes
  • positively charged homochiral cyclic trinuclear metallacalix[3]arene species
[Definition]

ChEBI: 4,7-phenanthroline is a phenanthroline.
[General Description]

4,7-Phenanthroline reacts with ruthenium carbonyl to yield cyclometalated derivatives.
[Enzyme inhibitor]

This hygroscopic reagent (FWfree-base = 180.21 g/mol; M.P. = 172-174°C; CAS 230-07-9), is a non-chelating isomer of 1,10-phenanthroline. Before inferring that the action of 1,10-phenanthroline is metal ion chelation, one should also assess the inhibitory effect of this non-chelating isomer. If a similar degree of inhibition is observed with both, one may assume that the effect has nothing to do with chelation an essential metal ion activator. See also 1,10-Phenanthroline; 1,-7Phenanthroline Target (s) : aldehyde dehydrogenase; leucyl aminopeptidase, weakly inhibited; nitrilase ; pyroglutamyl-peptidase II, or thyrotropin-releasing-hormone-degrading ectoenzyme.
Spectrum DetailBack Directory
[Spectrum Detail]

4,7-PHENANTHROLINE(230-07-9)1HNMR
4,7-PHENANTHROLINE(230-07-9)IR1
4,7-PHENANTHROLINE(230-07-9)Raman
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