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2,6-Pyridinedicarboxylic acid, mono(phenylmethyl) ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

125686-90-0

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125686-90-0 Usage

Appearance

White to off-white solid

Solubility

Sparingly soluble in water, but soluble in organic solvents

Common Uses

Intermediate in the synthesis of pharmaceuticals and agrochemicals
Building block in the production of various organic compounds

Reactivity

Versatile in chemical reactions

Handling Precautions

Should be handled with caution
Use in a well-ventilated area
Wear appropriate protective equipment

Health Hazards

Potential health hazards associated

Check Digit Verification of cas no

The CAS Registry Mumber 125686-90-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,6,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 125686-90:
(8*1)+(7*2)+(6*5)+(5*6)+(4*8)+(3*6)+(2*9)+(1*0)=150
150 % 10 = 0
So 125686-90-0 is a valid CAS Registry Number.

125686-90-0SDS

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 6-phenylmethoxycarbonylpyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names 6-((benzyloxy)carbonyl)picolinic 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:125686-90-0 SDS

125686-90-0Relevant academic research and scientific papers

Ultra-thin films of amphiphilic lanthanide complexes: multi-colour emission from molecular monolayers

Harrison, John A.,Kitchen, Jonathan A.,O’Neil, Alex T.

, p. 8067 - 8070 (2021)

We report the synthesis and Langmuir-Blodgett deposition of 4 brightly emissive lanthanide amphiphiles that can be co-deposited to give multi-emissive ultra-thin films where two, three and four distinct lanthanide emission profiles are observed. To the be

Exploring the Effect of Ligand Structural Isomerism in Langmuir–Blodgett Films of Chiral Luminescent EuIIISelf-Assemblies

Galanti, Agostino,Kotova, Oxana,Blasco, Salvador,Johnson, Chloe J.,Peacock, Robert D.,Mills, Shaun,Boland, John J.,Albrecht, Martin,Gunnlaugsson, Thorfinnur

, p. 9709 - 9723 (2016)

Here we have investigated the influence of the antenna group position on both the formation of chiral amphiphilic EuIII-based self-assemblies in CH3CN solution and, on the ability to form monolayers on the surface of quartz substrate

The application of chiroptical spectroscopy (circular dichroism) in quantifying binding events in lanthanide directed synthesis of chiral luminescent self-assembly structures

Kotova, Oxana,Blasco, Salvador,Twamley, Brendan,O'Brien, John,Peacock, Robert D.,Kitchen, Jonathan A.,Martnez-Calvo, Miguel,Gunnlaugsson, Thorfinnur

, p. 457 - 471 (2015)

The binding of asymmetrical and optically pure tridentate ligands (L = 1(S) and 1(R)) containing one carboxylic group and 2-naphthyl as an antenna to lanthanide ions (M = La(iii) and Eu(iii)) was studied in CH3CN, showing the successive formati

Luminescent lanthanide (Eu(iii)) cross-linked supramolecular metallo co-polymeric hydrogels: The effect of ligand symmetry

Bradberry, Samuel J.,Dee, Garret,Kotova, Oxana,McCoy, Colin P.,Gunnlaugsson, Thorfinnur

supporting information, p. 1754 - 1757 (2019/02/12)

Two lanthanide luminescent naphthyl-dipicolinic amide (dpa) methacrylate monomers for the synthesis of grafted supramolecular co-polymer gels (hydrogels), and their use as additional crosslinks in robust covalently cross-linked HEMA hydrogels is presented

The effect of the linker size in C2-symmetrical chiral ligands on the self-assembly formation of luminescent triple-stranded di-metallic Eu(iii) helicates in solution

Kotova, Oxana,Comby, Steve,Pandurangan, Komala,Stomeo, Floriana,O'Brien, John E.,Feeney, Martin,Peacock, Robert D.,McCoy, Colin P.,Gunnlaugsson, Thorfinnur

supporting information, p. 12308 - 12317 (2018/09/25)

Chiral lanthanide-based supramolecular structures have gained significant importance in view of their application in imaging, sensing and other functional purposes. We have designed chiral C2-symmetrical ligands (L) based on the use of two 2,6-

IRAK4 INHIBITING AGENTS

-

Page/Page column 125; 126, (2016/03/13)

Provided are compounds of Formula (I), or pharmaceutically acceptable salts thereof, and methods for their use and production.

COMPOUNDS AND METHODS for the inhibition of HDAC

-

Paragraph 0447-0448, (2015/11/24)

Disclosed are compounds having the formula: wherein X1, X2, X3, R1, R2, R3, R4, Y, A, Z, L and n are as defined herein, and methods of making and using the same.

HIV INTEGRASE INHIBITORS

-

Page/Page column 70, (2012/08/27)

Provided herein, inter alia, are novel compounds for the inhibition of HIV integrase. The compounds disclosed herein are useful for methods of treating HIV infection in a subject in need thereof.

4,6-DISUBSTITUTED PYRIMIDINES AND THEIR USE AS PROTEIN KINASE INHIBITORS

-

Page/Page column 58, (2008/06/13)

The invention relates to novel pyrimidine derivatives of Formula (I), which are efficacious inhibitors of protein kinases, in particular of one or more isoforms of the protein kinase B/Akt.

Novel folding patterns in a family of oligoanthranilamides: Non-peptide oligomers that form extended helical secondary structures

Hamuro, Yoshitomo,Geib, Steven J.,Hamilton, Andrew D.

, p. 10587 - 10593 (2007/10/03)

Anthranilamide derivatives are used as the basis for a series of novel oligomers that fold into helical secondary structures in the solid state. When combined with pyridine-2,6-dicarboxylic acid and 4,6-dimethoxy-1,3-diaminobenzene subunits, oligoanthrani

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