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14920-87-7

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14920-87-7 Usage

General Description

Methyl 2,6-dichlorobenzoate is a synthetic organic chemical compound characterized by the formula C8H6Cl2O2. METHYL 2,6-DICHLOROBENZOATE falls under the category of dichlorobenzoates and is composed of a benzoate ester pendant to which two chlorine atoms are attached at positions 2 and 6 of the benzene ring. It has a molecular weight of 221.04 g/mol. The compound is commonly used in the synthesis of various chemical products, especially in the fields of medicine and agrochemicals. Despite its broad usage, the detailed properties, including the detailed toxicological properties of the methyl 2,6-dichlorobenzoate, are not well-studied and thus it should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 14920-87-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,9,2 and 0 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 14920-87:
(7*1)+(6*4)+(5*9)+(4*2)+(3*0)+(2*8)+(1*7)=107
107 % 10 = 7
So 14920-87-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H6Cl2O2/c1-12-8(11)7-5(9)3-2-4-6(7)10/h2-4H,1H3

14920-87-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name METHYL 2,6-DICHLOROBENZOATE

1.2 Other means of identification

Product number -
Other names 2,6-Dichlor-benzoesaeure-methylester

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:14920-87-7 SDS

14920-87-7Relevant articles and documents

Visible-light-induced selective aerobic oxidation of sp3 C-H bonds catalyzed by a heterogeneous AgI/BiVO4 catalyst

Jiang, Li-Ya,Ming, Jing-Jing,Wang, Lian-Yue,Jiang, Yuan-Yuan,Ren, Lan-Hui,Wang, Zi-Cheng,Cheng, Wen-Chen

supporting information, p. 1156 - 1163 (2020/03/11)

An efficient oxidation of sp3 C-H bonds to esters and ketones has been developed using AgI/BiVO4 as the photocatalyst and O2 as the oxidant in water. Various substrates can be transformed into the desired esters and ketones in moderate to good yields. The synthetic utility of this approach has been demonstrated by gram-level experiments and consecutive oxidation experiments. A plausible mechanism has been proposed.

Methyl group transfer upon gas phase decomposition of protonated methyl benzoate and similar compounds

Frański, Rafa?,Gierczyk, B?a?ej,Zalas, Maciej,Jankowski, Wojciech,Hoffmann, Marcin

, p. 379 - 384 (2018/05/14)

Gas phase decompositions of protonated methyl benzoate and its conjugates have been studied by using electrospray ionization-collision induced dissociation-tandem mass spectrometry. Loss of CO2 molecule, thus transfer of methyl group, has been observed. In order to better understand this process, the theoretical calculations have been performed. For methyl benzoate conjugates, it has been found that position of substituent affects the loss of CO2 molecule, not the electron donor/withdrawing properties of the substituent. Therefore, electrospray ionization-mass spectrometry in positive ion mode may be useful for differentiation of isomers of methyl benzoate conjugates.

The dual role of ionic liquid BmimBF4, precursor of N-heterocyclic carbene and solvent, in the oxidative esterification of aldehydes

Chiarotto, Isabella,Feroci, Marta,Sotgiu, Giovanni,Inesi, Achille

, p. 8088 - 8095 (2013/08/23)

Room temperature ionic liquid BmimBF4 (1-butyl-3- methylimidazolium tetrafluoroborate) has been utilized in the N-heterocyclic carbene-catalyzed oxidation of aldehydes to yield esters. In the presence of MnO2 as oxidant and of DBU and caesium carbonate as bases, aromatic, heteroaromatic and aliphatic esters have been isolated in good to excellent yields. The recyclability of the used ionic liquid along with the excess of inorganic reagents has been proved. The simple and cheap BmimBF4 ionic liquid played the dual role of precatalyst and solvent. This is the first time that such a reaction has been carried out with an ionic liquid as solvent.

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