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3-(dimethylamino)-1-(phenanthren-3-yl)propan-1-one is a complex organic compound with the molecular formula C19H21NO. It features a phenanthren-3-yl group attached to a propanone (ketone) moiety, with a dimethylamino group at the 3-position. 3-(dimethylamino)-1-(phenanthren-3-yl)propan-1-one is characterized by its aromatic structure, which includes a phenanthrene ring system, and its basic nitrogen functionality due to the dimethylamino group. It is likely to be a colorless solid and may exhibit properties such as low solubility in water and higher solubility in organic solvents. The compound could be used in various chemical applications, including the synthesis of pharmaceuticals, dyes, or other organic compounds, due to its unique structure and reactivity.

7470-59-9

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7470-59-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7470-59-9 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, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7470-59:
(6*7)+(5*4)+(4*7)+(3*0)+(2*5)+(1*9)=109
109 % 10 = 9
So 7470-59-9 is a valid CAS Registry Number.

7470-59-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(dimethylamino)-1-phenanthren-3-ylpropan-1-one,hydrochloride

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

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More Details:7470-59-9 SDS

7470-59-9Downstream Products

7470-59-9Relevant 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.

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