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Phenol, 2,6-dinitro-, benzoate (ester) is a chemical compound derived from phenol, a simple aromatic molecule. In Phenol, 2,6-dinitro-, benzoate (ester), two nitro groups are attached to the phenol ring at the 2nd and 6th positions, and a benzoate group is esterified to the hydroxyl group of the phenol. The chemical structure can be represented as C13H9NO6. Phenol, 2,6-dinitro-, benzoate (ester) is an organic ester with potential applications in chemical research and synthesis. It is important to note that due to the presence of nitro groups, Phenol, 2,6-dinitro-, benzoate (ester) may exhibit explosive properties and should be handled with caution. Additionally, the compound may have potential uses in the synthesis of dyes, pharmaceuticals, or other organic compounds, but specific applications would depend on further research and development.

1523-16-6

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1523-16-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1523-16-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,2 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1523-16:
(6*1)+(5*5)+(4*2)+(3*3)+(2*1)+(1*6)=56
56 % 10 = 6
So 1523-16-6 is a valid CAS Registry Number.

1523-16-6SDS

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 2,6-dinitrophenyl benzoate

1.2 Other means of identification

Product number -
Other names benzoic acid-(2,6-dinitro-phenyl 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:1523-16-6 SDS

1523-16-6Relevant academic research and scientific papers

Ph3P-I2 mediated aryl esterification with a mechanistic insight

Phakhodee, Wong,Duangkamol, Chuthamat,Pattarawarapan, Mookda

supporting information, p. 2087 - 2089 (2016/04/26)

In order to better understand the reaction mechanism and to obtain optimal conditions, the Ph3P-I2/Et3N mediated aryl esterification reaction was thoroughly investigated. Using a specific reagent addition sequence, the reaction proceeds remarkably well especially with acidic substrates. 31P NMR studies revealed that the formation of an aryloxyphosphonium salt is crucial in governing the reaction path toward the formation of phenolic esters.

17O NMR study of ortho and alkyl substituent effects in substituted phenyl and alkyl esters of benzoic acids

Nummert, Vilve,Maeemets, Vahur,Piirsalu, Mare,Vahur, Signe,Koppel, Ilmar A.

experimental part, p. 1737 - 1763 (2012/04/17)

17O NMR spectra for 44 ortho-, meta- and para-substituted phenyl and alkyl benzoates (C6H5CO2C 6H4-X, C6H5CO2R) at natural abundance in acetonitrile were re

Mechanism of catalysis with triethylamine of phenols benzoylation in dioxane. New quality experiment

Belousova,Simanenko,Savelova,Suprun

, p. 1656 - 1664 (2007/10/03)

Acylation kinetics with benzoyl chloride in the presence of triethylamine in dioxane at 25°C was studied for substituted nitrophenols (R = 2,4,6-(NO2)3, 2,5-(NO2)2, 2,4-(NO2)2, 4-NO2/

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