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2-(2,4-dichlorophenoxy)-5-nitropyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

28232-31-7

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28232-31-7 Usage

Physical form

Yellow crystalline solid

Uses

Intermediate in the synthesis of pharmaceuticals and other organic compounds, herbicidal properties (used in the production of herbicides)

Chemical structure

Includes both a pyridine and a phenol ring, making it a nitrophenol derivative

Hazardous nature

Considered hazardous if inhaled, ingested, or comes into contact with skin, appropriate safety measures should be taken when handling it.

Check Digit Verification of cas no

The CAS Registry Mumber 28232-31-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,2,3 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 28232-31:
(7*2)+(6*8)+(5*2)+(4*3)+(3*2)+(2*3)+(1*1)=97
97 % 10 = 7
So 28232-31-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H6Cl2N2O3/c12-7-1-3-10(9(13)5-7)18-11-4-2-8(6-14-11)15(16)17/h1-6H

28232-31-7SDS

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-(2,4-dichlorophenoxy)-5-nitropyridine

1.2 Other means of identification

Product number -
Other names 2-(2,4-Dichlor-phenoxy)-5-nitro-pyridin

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:28232-31-7 SDS

28232-31-7Downstream Products

28232-31-7Relevant academic research and scientific papers

Convenient Synthesis of Phenyl Pyridylethers Utilizing Fluoride Ion

Hwang, Ki-Jun,Park, Seung Ki

, p. 949 - 954 (2007/10/02)

Aryl pyridyl ethers were prepared from phenols and active halopyridines under essentially neutral condition via fluoride ion assisted reaction.

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