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459856-12-3

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459856-12-3 Usage

General Description

2-Methyl-6-methoxypyridine-3-boronic acid is a chemical compound with the molecular formula C8H10BNO3. It is a boronic acid derivative that contains a pyridine ring with a methyl and methoxy group attached to it. 2-METHYL-6-METHOXYPYRIDINE-3-BORONIC ACID is commonly used in organic synthesis and pharmaceutical research as a building block for the construction of various biologically active molecules. It is also used as a reagent in the Suzuki-Miyaura coupling reaction, a widely used chemical reaction for the formation of carbon-carbon bonds. 2-Methyl-6-methoxypyridine-3-boronic acid is considered to be a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and other fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 459856-12-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,8,5 and 6 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 459856-12:
(8*4)+(7*5)+(6*9)+(5*8)+(4*5)+(3*6)+(2*1)+(1*2)=203
203 % 10 = 3
So 459856-12-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H10BNO3/c1-5-6(8(10)11)3-4-7(9-5)12-2/h3-4,10-11H,1-2H3

459856-12-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-6-methoxypyridine-3-boronic acid

1.2 Other means of identification

Product number -
Other names (6-methoxy-2-methylpyridin-3-yl)boronic acid

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:459856-12-3 SDS

459856-12-3Relevant articles and documents

Fluorine-free blue-green emitters for light-emitting electrochemical cells

Evariste, Sloane,Sandroni, Martina,Rees, Thomas W.,Roldan-Carmona, Cristina,Gil-Escrig, Lidon,Bolink, Henk J.,Baranoff, Etienne,Zysman-Colman, Eli

, p. 5793 - 5804 (2014/07/22)

There is presently a lack of efficient and stable blue emitters for light-emitting electrochemical cells (LEECs), which limits the development of white light emitting systems for lighting. Cyclometalated iridium complexes as blue emitters tend to show low photoluminescence efficiency due to significant ligand-centred character of the radiative transition. The most common strategy to blue-shift the emission is to use fluorine substituents on the cyclometalating ligand, such as 2,4-difluorophenylpyridine, dFppy, which has been shown to decrease the stability of the emitter in operating devices. Herein we report a series of four new charged cyclometalated iridium complexes using methoxy- and methyl-substituted 2,3′-bipyridine as the main ligands. The combination of donor groups and the use of a cyclometalated pyridine has been recently reported for neutral complexes and found electronically equivalent to dFppy. We describe the photophysical and electrochemical properties of the complexes in solution and use DFT and TDDFT calculations to gain insights into their properties. The complexes exhibit bluish-green emission with onsets around 450 nm, which correspond to the maximum emission at 77 K. Furthermore, photoluminescence quantum yields in solution are all above 40%, with the brightest in the series at 66%. Finally, LEECs were prepared using these complexes as the emissive material to evaluate the performance of this particular design. Compared to previously reported devices with fluorine-containing emitters, the emitted colours are slightly red-shifted due to methyl substituents on the coordinating pyridine of the main ligand and overall device performances, unfortunately including the stability of devices, are similar to those previously reported. Interestingly within the series of complexes there appears to be a positive effect of the methoxy-substituents on the stability of the devices. The poor stability is therefore attributed to the combination of cyclometalated pyridine and methoxy groups. the Partner Organisations 2014.

1-(PIPERIDIN-4-YL)-1H-INDOLE DERIVATIVE

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Page/Page column 123-124, (2010/11/28)

The present invention provides a compound represented by the formula (1) or a pharmacologically acceptable salt thereof, or a hydrate thereof (provided that a compound in which all of R4a, R4b, and R4c are hydrogen atoms is excluded.): [wherein R1 represents a hydrogen atom, R2 represents a hydrogen atom, R3 represents the formula: wherein R4a, R4b, and R4c are the same as or different from each other and each represents a hydrogen atom, a C1-6 alkyl group or a C1-6 alkoxy group, etc.]

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