Welcome to LookChem.com Sign In|Join Free
  • or
Acridine, 9-[4-(bromomethyl)phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

183170-02-7

Post Buying Request

183170-02-7 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

183170-02-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 183170-02-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,3,1,7 and 0 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 183170-02:
(8*1)+(7*8)+(6*3)+(5*1)+(4*7)+(3*0)+(2*0)+(1*2)=117
117 % 10 = 7
So 183170-02-7 is a valid CAS Registry Number.

183170-02-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 9-[4-(bromomethyl)phenyl]acridine

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

1.5 Emergency phone number

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

More Details:183170-02-7 SDS

183170-02-7Upstream product

183170-02-7Downstream Products

183170-02-7Relevant academic research and scientific papers

Control of electron-transfer and DNA binding properties by the tolyl spacer group in viologen linked acridines

Joseph, Joshy,Eldho, Nadukkudy V.,Ramaiah, Danaboyina

, p. 4444 - 4450 (2007/10/03)

Novel water soluble viologen and pyridinium linked tolylacridines 1a,b and 2a,b were synthesized and their photophysical and DNA binding properties including the photoinduced electron-transfer reactions were investigated. When compared to the cases of the model tolylacridines 3a,b and the pyridinium linked derivatives 2a,b, the singlet excited states of 1a and 1b were efficiently quenched in water and methanol. Intramolecular quenching rate constants (kET) calculated in water are found to be 1.2 × 1010 and 8.8 × 1010 s-1 for 1a and 1b and 1.4 × 108 and 0.9 × 108 s-1 for 2a and 2b, respectively, suggesting thereby that the viologen moiety quenches the fluorescence of the acridine chromophore efficiently when compared to the case of the pyridinium moiety. From the intermolecular electron-transfer studies, it was observed that the singlet and triplet excited states of the acridine chromophore are capable of donating an electron to the viologen moiety. DNA binding studies indicated that the p-tolylachridine derivatives 1a and 2a exhibit strong binding to DNA with binding constants of 1.0 × 105 and 3.3 × 105 M-1, respectively, whereas the o-tolylacridine derivatives 1b and 2b showed negligible affinity for DNA. The rate constants for the static quenching of 1a and 2a by DNA (kDNA) are found to be 7 × 109 and 3 × 109 s-1, respectively, indicating that 1a is an efficient DNA oxidizing agent. Nanosecond laser flash photolysis studies of these systems in aqueous solutions did not show any transients. However, in the presence of DNA, 1a gave transient absorption due to the reduced methyl viologen radical cation. These results demonstrate that the tolyl spacer group in these systems constitutes an interesting variation which controls both the electron transfer and DNA binding properties, and hence, such molecules and derivatives thereof can have potential application as probes for nucleic acids and as DNA cleaving agents.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 183170-02-7