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Chlorquinox is a quinoxaline antifungal agent characterized by the replacement of hydrogens at positions 5, 6, 7, and 8 with chlorines. It was developed in the 1970s and was historically utilized in agriculture for the control of powdery mildew on crops. However, its use has become obsolete in recent times.

3495-42-9

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3495-42-9 Usage

Uses

Used in Agricultural Industry:
Chlorquinox was used as a fungicide for the control of powdery mildew in crops. Its application aimed to protect plants from fungal infections, ensuring a healthy growth and yield. However, due to its obsolescence, it is no longer used in this capacity today.

Check Digit Verification of cas no

The CAS Registry Mumber 3495-42-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,4,9 and 5 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3495-42:
(6*3)+(5*4)+(4*9)+(3*5)+(2*4)+(1*2)=99
99 % 10 = 9
So 3495-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H2Cl4N2/c9-3-4(10)6(12)8-7(5(3)11)13-1-2-14-8/h1-2H

3495-42-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name chlorquinox

1.2 Other means of identification

Product number -
Other names 5,6,7,8-Tetrachlor-chinoxalin

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:3495-42-9 SDS

3495-42-9Downstream Products

3495-42-9Relevant academic research and scientific papers

Halogenated (F, Cl) 1,3-benzodiazoles, 1,2,3-benzotriazoles, 2,1,3-benzothia(selena)diazoles and 1,4-benzodiazines inducing Hep2 cell apoptosis

Prima, Darya O.,Vorontsova, Elena V.,Makarov, Arkady G.,Makarov, Alexander Yu.,Bagryanskaya, Irina Yu.,Mikhailovskaya, Tatiana F.,Slizhov, Yuri G.,Zibarev, Andrey V.

, p. 439 - 442 (2017/10/05)

The title compounds synthesized from halogenated arene-1,2-diamines revealed, together with the latter, cytotoxicity towards the Hep2 (laryngeal epidermoid carcinoma) cells. The cytotoxicity was high and was accompanied by pronounced apoptotic activity at

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