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4-Acridinecarboxylic acid, 9-chloro-, 4-nitrophenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63178-95-0

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63178-95-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63178-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,7 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 63178-95:
(7*6)+(6*3)+(5*1)+(4*7)+(3*8)+(2*9)+(1*5)=140
140 % 10 = 0
So 63178-95-0 is a valid CAS Registry Number.

63178-95-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl) 9-chloroacridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-Acridinecarboxylic acid,9-chloro-,4-nitrophenyl ester

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:63178-95-0 SDS

63178-95-0Downstream Products

63178-95-0Relevant academic research and scientific papers

Acridinecarboxamide compounds

-

, (2008/06/13)

4-Carboxamidoacridine compounds represented by the general formula (I), STR1 where R1 represents H, CH3 or NHR3, where R3 is H, COCH3, SO2 CH3, COPh, SO2 Ph or lower alkyl optionally substituted with hydroxyl and/or amino functions; R2 represents H or up to two of the groups CH3, OCH3, halogen, CF3, NO2, NH2, NHCOCH3, and NHCOOCH3 placed at positions 1-3 or 5-8; Y represents C(NH)NH2, NHC(NH)NH2, or NR4 R5, where each of R4 and R5 is H or lower alkyl optionally substituted with hydroxyl and/or amino functions; and x is from 2 to 6, and the acid addition salts thereof, possess antibacterial and antitumor properties.

Potential antitumor agents. 43. Synthesis and biological activity of dibasic 9-aminoacridine-4-carboxamides, a new class of antitumor agent

Atwell,Cain,Baguley,Finlay,Denny

, p. 1481 - 1485 (2007/10/02)

The synthesis and biological activities of representatives of a new class of antitumor agent, the N-[2-(dialkyl-amino)ethyl-9-aminoacridine-4-carboxamides, are reported. Members of this class are stable and very water soluble with high levels of in vitro

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