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678015

Sigma-Aldrich

4,7-Dichloro-1,10-phenanthroline

97%

Synonym(s):

4,7-Dichloro-o-phenanthroline

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About This Item

Empirical Formula (Hill Notation):
C12H6Cl2N2
CAS Number:
5394-23-0
Molecular Weight:
249.10
MDL number:
MFCD00233882
UNSPSC Code:
12352300
PubChem Substance ID:
24885412
NACRES:
NA.22

Assay

97%

form

solid

mp

243-247 °C

SMILES string

Clc1ccnc2c1ccc3c(Cl)ccnc23

InChI

1S/C12H6Cl2N2/c13-9-3-5-15-11-7(9)1-2-8-10(14)4-6-16-12(8)11/h1-6H

InChI key

GIEQBYJCGYHHSU-UHFFFAOYSA-N

Pictograms

Skull and crossbonesCorrosion
GHS06,GHS05

Signal Word

Danger

Hazard Statements

H301,H315,H318,H335

Hazard Classifications

Acute Tox. 3 Oral - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

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)

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Ryan A Altman et al.
Organic letters, 8(13), 2779-2782 (2006-06-16)
[reaction: see text] 4,7-Dimethoxy-1,10-phenanthroline (L) was found to be an efficient ligand for the copper-catalyzed N-arylation of imidazole with aryl iodides and bromides under mild conditions. A variety of hindered and functionalized imidazoles and aryl halides were transformed in good
Anna M Maroń et al.
Dalton transactions (Cambridge, England : 2003), 49(14), 4441-4453 (2020-03-18)
Three Re(i) carbonyl complexes [ReCl(CO)3(Ln)] bearing 2,2'-bipyridine, 2,2':6',2''-terpyridine, and 1,10-phenanthroline functionalized with diphenylamine/or triphenylamine units (L1-L3) were synthesized to explore the impact of highly electron donating units appended to the imine ligand on the thermal and optoelectronic properties of Re(i)

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