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9-Acridinamine, 2-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

23045-35-4

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23045-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23045-35-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,0,4 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23045-35:
(7*2)+(6*3)+(5*0)+(4*4)+(3*5)+(2*3)+(1*5)=74
74 % 10 = 4
So 23045-35-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H9N3O2/c14-13-9-3-1-2-4-11(9)15-12-6-5-8(16(17)18)7-10(12)13/h1-7H,(H2,14,15)

23045-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-nitroacridin-9-amine

1.2 Other means of identification

Product number -
Other names 9-Amino-2-nitroacridine

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:23045-35-4 SDS

23045-35-4Downstream Products

23045-35-4Relevant academic research and scientific papers

NOVEL FLUORESCENT DYES AND USES THEREOF

-

, (2014/04/04)

The present invention relates to fluorescent dyes based on acridine derivatives and use of such dyes, for example, in biochemical and/or cell based assays. A preferred feature of some of the dyes described is their long fluorescence lifetimes and their us

Enhancement of mutagenic activity of 9-aminoacridine by introducing a nitro group into the molecule.

Tomosaka,Omata,Anzai

, p. 1420 - 1423 (2007/10/02)

Mutagenic activity and DNA intercalation were examined for 9-aminoacridine (9-AA) and its derivatives. Introduction of a nitro group into the 9-AA molecule was found to enhance the activity enormously as was detected by the Ames test. Acetylation of amino group at 9-position of acridine ring inhibited the intercalation, the frameshift activity disappearing. Rat liver S9 converted 9-AA metabolically to 9-amino-2-hydroxyacridine.

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