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7-Nitroquinolin-2-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

49609-04-3

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49609-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 49609-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,6,0 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 49609-04:
(7*4)+(6*9)+(5*6)+(4*0)+(3*9)+(2*0)+(1*4)=143
143 % 10 = 3
So 49609-04-3 is a valid CAS Registry Number.

49609-04-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-nitroquinolin-2-amine

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:49609-04-3 SDS

49609-04-3Downstream Products

49609-04-3Relevant academic research and scientific papers

7-Aminoquinolines. A novel class of agents active against herpesviruses

Nasr,Drach,Smith,Shipman Jr.,Burckhalter

, p. 1347 - 1351 (2007/10/02)

A series of 7-aminoquinoline derivatives was synthesized and evaluated for their capacity to produce cytotoxicity in KB cells and to inhibit the replication of herpes simplex virus (HSV) type 1. All compounds tested inhibited the replication of HSV-1 with 50% inhibitory concentrations in the range of 2-50 μg/mL. The antiviral activity of many compounds, however, was separated from cytotoxicity to replicating uninfected cells by only two- to fivefold higher than those required for antiviral activity. Nonetheless, six compounds (10, 28, 29, 32, 34, and 36) were identified in which the separation was greater than fivefold. All compounds examined were more potent inhibitors of viral DNA synthesis than the cellular DNA synthesis.

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