7470-69-1 Usage
Molecular structure
The compound consists of a phenanthrene group and a piperidine group connected to a propanone backbone.
Molecular weight
Approximately 329.44 g/mol
Appearance
It is likely a solid or crystalline substance, although the exact appearance may vary depending on the conditions.
Solubility
The solubility of 1-(phenanthren-3-yl)-3-(piperidin-1-yl)propan-1-one is not explicitly mentioned, but it may be soluble in organic solvents such as ethanol, methanol, or acetone due to its nonpolar nature.
Stability
The stability of the compound is not explicitly mentioned, but it is generally stable under normal laboratory conditions.
Reactivity
1-(phenanthren-3-yl)-3-(piperidin-1-yl)propan-1-one is likely to be reactive in various chemical reactions and organic synthesis processes due to its molecular structure.
Uses
It is often used in research and laboratory settings as a precursor for the synthesis of other compounds and pharmaceuticals.
Safety precautions
It is important to handle this chemical with care and follow safety guidelines when working with it in a laboratory setting. This may include wearing appropriate personal protective equipment (PPE), such as gloves, goggles, and a lab coat, and working in a well-ventilated area.
Storage
The compound should be stored in a cool, dry, and dark place, preferably in a sealed container to protect it from light, moisture, and air.
Check Digit Verification of cas no
The CAS Registry Mumber 7470-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,7 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7470-69:
(6*7)+(5*4)+(4*7)+(3*0)+(2*6)+(1*9)=111
111 % 10 = 1
So 7470-69-1 is a valid CAS Registry Number.
7470-69-1Relevant academic research and scientific papers
Evaluation of alkylating and intercalating properties of mannich bases for cytotoxic activity
Istanbullu, Huseyin,Erzurumlu, Yalcin,Kirmizibayrak, Petek Ballar,Erciyas, Ercin
, p. 1096 - 1106 (2015/04/14)
A series of new "hybrid compounds", Mannich base derivatives of planar polycyclic/heterocyclic starting materials, was designed and synthesized. The structures of the compounds were confirmed by spectroscopic methods and elemental analysis. Cytotoxicity of compounds was investigated in three cancer cell lines (PC3, HeLa, and MCF7) and one non-tumoral cell line (293 HEK). We tested the DNA-intercalating capability of the molecules by ethidium bromide (EtBr) fluorescence displacement experiment. Compounds' alkylation potency was investigated via in vitro incubation test using 2-mercaptoethanol, a biomimetic nucleophile. The five of the compounds (7s, 9d, 10b, 11b, 12c) are reported for first time in the literature. Our results suggest that compound 9d has a biological activity close to the reference compound doxorubicin, an intercalating agent in clinical use.
