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9-[(2Z)-2-(1-phenylethylidene)hydrazinyl]acridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

97869-47-1

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97869-47-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97869-47-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,6 and 9 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97869-47:
(7*9)+(6*7)+(5*8)+(4*6)+(3*9)+(2*4)+(1*7)=211
211 % 10 = 1
So 97869-47-1 is a valid CAS Registry Number.

97869-47-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[(Z)-1-phenylethylideneamino]acridin-9-amine

1.2 Other means of identification

Product number -
Other names Ethanone,1-phenyl-,9-acridinylhydrazone

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:97869-47-1 SDS

97869-47-1Downstream Products

97869-47-1Relevant academic research and scientific papers

Novel carbohydrazide and hydrazone biomarkers based on 9-substituted acridine and anthracene fluorogens

Bedlcoviova, Zdenka,Imrich, Jn,Kristian, Pavol,Danihel, Ivan,Boehm, Stanislav,Sabolova, Danica,Kozurkova, Maria,Paulikova, Helena,Klika, Karel D.

experimental part, p. 1047 - 1066 (2010/10/21)

Three series of carbohydrazides or hydrazones bearing either acridine or anthracene pharmacophores were synthesized as potential noncovalent DNA-binding antitumor agents. Carbohydrazides with an acridine or anthracene moiety were prepared from appropriate acridine or anthracene carbaldehydes via cyclocondensation with selected hydrazides whilst hydrazones with a 10H-acridin-9-ylidene moiety were obtained by condensation of (acridin-9-yl)hydrazine with various aldehydes or ketones. The spectroscopic properties of the first two series revealed efficient fluorescence implying that the compounds could be amenable for use as biomarkers. The structures of the compounds were characterized by spectral methods (UV-vis, fluorescence, IR, and 1H, 13C, and 2D NMR) and quantum-chemical calculations (DFT, ZINDO, and AM1). The first carbohydrazide series was also tested against human leukemia cell line HL-60 wherein the phenyl-substituted derivative was found to possess the highest activity.

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