ChemicalBook--->CAS DataBase List--->187173-05-3

187173-05-3

187173-05-3 Structure

187173-05-3 Structure
IdentificationBack Directory
[Name]

2-(4,5-DIHYDROIMIDAZOL-2-YL)QUINOLINE HYDROCHLORIDE
[CAS]

187173-05-3
[Synonyms]

BU 224 HYDROCHLORIDE
Quinoline, 2-(4,5-dihydro-1H-imidazol-2-yl)-
2-(4,5-DIHYDROIMIDAZOL-2-YL)QUINOLINE HYDROCHLORIDE
[Molecular Formula]

C12H11N3
[MDL Number]

MFCD00467639
[MOL File]

187173-05-3.mol
[Molecular Weight]

197.24
Chemical PropertiesBack Directory
[Boiling point ]

372.9±34.0 °C(Predicted)
[density ]

1.27±0.1 g/cm3(Predicted)
[storage temp. ]

Desiccate at RT
[solubility ]

ethanol: 1.2 mg/mL
[form ]

solid
[pka]

9.87±0.40(Predicted)
[color ]

white
[InChI]

1S/C12H11N3.ClH/c1-2-4-10-9(3-1)5-6-11(15-10)12-13-7-8-14-12;/h1-6H,7-8H2,(H,13,14);1H
[InChIKey]

DDFHQXAQWZWRSQ-UHFFFAOYSA-N
[SMILES]

Cl[H].C1CN=C(N1)c2ccc3ccccc3n2
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Hazard InformationBack Directory
[Uses]

BU224 is one of the two most widely studied I2 receptor ligands and have antinociceptive and antidepressant-?like activities in rodents.
[Biological Activity]

High affinity ligand for the imidazoline I 2 binding site (K i = 2.1 nM). Putative I 2 antagonist; antagonizes the effects of imidazoline ligands on morphine antinociception. Produces ipsiversive rotational behavior in rats with a full 6-OHDA lesion of the nigrostriatal tract.
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