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Methyl 2-(2,4-dinitrophenoxy)benzoate is a chemical compound with the molecular formula C15H11N2O7. It is an ester derivative of 2-(2,4-dinitrophenoxy)benzoic acid, where the hydroxyl group is replaced by a methyl group. This yellow crystalline solid is known for its use as a chemical intermediate in the synthesis of various pharmaceuticals and agrochemicals. It is also recognized for its potential applications in the development of dyes and pigments. The compound is characterized by its reactivity and can be involved in various chemical reactions, making it a versatile component in organic chemistry.

2363-41-9

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2363-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2363-41-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,3,6 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2363-41:
(6*2)+(5*3)+(4*6)+(3*3)+(2*4)+(1*1)=69
69 % 10 = 9
So 2363-41-9 is a valid CAS Registry Number.

2363-41-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 2-(2,4-dinitrophenoxy)benzoate

1.2 Other means of identification

Product number -
Other names 2-(2,4-dinitro-phenoxy)-benzoic acid methyl 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:2363-41-9 SDS

2363-41-9Relevant academic research and scientific papers

Synthesis and antimycobacterial activity of nitroxanthones. 1st Communication: Synthesis and differential scanning calorimetry analysis

Ibrom, Wolfgang G. A.,Frahm, August W.

, p. 662 - 667 (2007/10/03)

The syntheses of mono-, di-, tri- and tetranitroxanthones via intramolecular Friedel-Crafts acylation of nitrated 2-phenoxybenzoic acids as well as via selective stepwise nitration of xanthone and the nitroxanthones gained from the first route are describ

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