Basic Information | Post buying leads | Suppliers | Cas Database |
Name |
2-(4-Nitrophenyl)imidazo[1,2-a]pyridine |
EINECS | N/A |
CAS No. | 3323-26-0 | Density | 1.34 g/cm3 |
PSA | 63.12000 | LogP | 3.43270 |
Solubility | N/A | Melting Point |
N/A |
Formula | C13H9N3O2 | Boiling Point | N/A |
Molecular Weight | 239.233 | Flash Point | N/A |
Transport Information | N/A | Appearance | N/A |
Safety | Risk Codes | N/A | |
Molecular Structure | Hazard Symbols | N/A | |
Synonyms |
Imidazo[1,2-a]pyridine,2-(p-nitrophenyl)- (7CI,8CI);2-(4-Nitrophenyl)imidazo[1,2-a]pyridine;Imidazo[1,2-a]pyridine,2-(4-nitrophenyl)-;2-(p-Nitrophenyl)imidazo(1,2-a)pyridine; |
Article Data | 37 |
The Imidazo(1,2-a)pyridine, 2-(p-nitrophenyl)-, with the CAS registry number 3323-26-0, is also known as 2-(p-Nitrophenyl)imidazo(1,2-a)pyridine. It belongs to the product category of Fused Ring Systems. This chemical's molecular formula is C13H9N3O2 and molecular weight is 239.23. What's more, its systematic name is 2-(4-nitrophenyl)imidazo[1,2-a]pyridine. Its classification code is Drug/Therapeutic Agent.
Physical properties of Imidazo(1,2-a)pyridine, 2-(p-nitrophenyl)- are: (1)ACD/LogP: 3.02; (2)# of Rule of 5 Violations: 0; (3)#H bond acceptors: 5; (4)#H bond donors: 0; (5)#Freely Rotating Bonds: 2; (6)Polar Surface Area: 63.12 Å2; (7)Index of Refraction: 1.686; (8)Molar Refractivity: 67.47 cm3; (9)Molar Volume: 177.2 cm3; (10)Polarizability: 26.75×10-24cm3; (11)Surface Tension: 59 dyne/cm; (12)Density: 1.34 g/cm3.
You can still convert the following datas into molecular structure:
(1)Canonical SMILES: C1=CC2=NC(=CN2C=C1)C3=CC=C(C=C3)[N+](=O)[O-]
(2)InChI: InChI=1S/C13H9N3O2/c17-16(18)11-6-4-10(5-7-11)12-9-15-8-2-1-3-13(15)14-12/h1-9H
(3)InChIKey: SNBCSKCONKUZBA-UHFFFAOYSA-N
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LD50 | intraperitoneal | 1500mg/kg (1500mg/kg) | BEHAVIORAL: SOMNOLENCE (GENERAL DEPRESSED ACTIVITY) BEHAVIORAL: IRRITABILITY | Journal of Medicinal Chemistry. Vol. 8, Pg. 305, 1965. |