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3-iodo-1,2-dihydroacenaphthylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24737-48-2

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24737-48-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24737-48-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,7,3 and 7 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 24737-48:
(7*2)+(6*4)+(5*7)+(4*3)+(3*7)+(2*4)+(1*8)=122
122 % 10 = 2
So 24737-48-2 is a valid CAS Registry Number.

24737-48-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-iodo-1,2-dihydroacenaphthylene

1.2 Other means of identification

Product number -
Other names 3-Jod-acenaphthen

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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:24737-48-2 SDS

24737-48-2Downstream Products

24737-48-2Relevant academic research and scientific papers

Synthesis and study of antiproliferative, antitopoisomerase II, DNA-intercalating and DNA-damaging activities of arylnaphthalimides

Quintana-Espinoza, Patricia,Garcia-Luis, Jonay,Amesty, Angel,Martin-Rodriguez, Patricia,Lorenzo-Castrillejo, Isabel,Ravelo, Angel G.,Fernandez-Perez, Leandro,Machin, Felix,Estevez-Braun, Ana

supporting information, p. 6484 - 6495 (2013/10/22)

A series of arylnaphthalimides were designed and synthesized to overcome the dose-limiting cytotoxicity of N-acetylated metabolites arising from amonafide, the prototypical antitumour naphthalimide whose biomedical properties have been related to its ability to intercalate the DNA and poison the enzyme Topoisomerase II. Thus, these arylnaphthalimides were first evaluated for their antiproliferative activity against two tumour cell lines and for their antitopoisomerase II in vitro activities, together with their ability to intercalate the DNA in vitro and also through docking modelization. Then, the well-known DNA damage response in Saccharomyces cerevisiae was employed to critically evaluate whether these novel compounds can damage the DNA in vivo. By performing all these assays we conclude that the 5-arylsubstituted naphthalimides not only keep but also improve amonafide's biological activities.

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