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6-(2-Methoxyphenyl)-picolinic acid is a chemical compound with the molecular formula C13H11NO3, belonging to the picolinic acid derivatives. It features a 2-methoxyphenyl group attached to the 6-position of the picolinic acid structure, which endows it with unique chemical and biological properties.

86696-69-7

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86696-69-7 Usage

Uses

Used in Metal Coordination Chemistry:
6-(2-Methoxyphenyl)-picolinic acid is used as a chelating agent for metal coordination chemistry. Its ability to form stable complexes with various metal ions makes it a valuable tool in the synthesis of metal-organic frameworks and coordination compounds with potential applications in catalysis, sensing, and materials science.
Used in Pharmaceutical Research:
6-(2-Methoxyphenyl)-picolinic acid is investigated for its potential pharmacological properties, including its anti-inflammatory and anti-tumor activities. Its unique structure allows it to modulate various biological pathways and target specific enzymes or receptors, making it a promising candidate for the development of new drugs.
Used in Synthesis of Novel Compounds:
6-(2-Methoxyphenyl)-picolinic acid is considered an important building block for the synthesis of novel compounds with potential biological and pharmaceutical activities. Its versatile chemical structure can be further modified or functionalized to create new molecules with improved properties or novel mechanisms of action.
Used in Chemical Research:
6-(2-Methoxyphenyl)-picolinic acid is utilized in various chemical research applications, such as studying the reactivity of its functional groups, exploring its coordination chemistry, or investigating its potential as a ligand in organometallic complexes.
Used in Analytical Chemistry:
6-(2-Methoxyphenyl)-picolinic acid can be employed as a reagent or a reference compound in analytical chemistry, particularly in the development of new methods for the detection, quantification, or separation of related compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 86696-69-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,6,9 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 86696-69:
(7*8)+(6*6)+(5*6)+(4*9)+(3*6)+(2*6)+(1*9)=197
197 % 10 = 7
So 86696-69-7 is a valid CAS Registry Number.

86696-69-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(2-methoxyphenyl)pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 6-(2-Methoxyphenyl)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:86696-69-7 SDS

86696-69-7Relevant academic research and scientific papers

A chiral picolinic acid ligand, Cl-NAPH-PyCOOH, for CPRU-catalyzed dehydrative allylation: Design, synthesis, and properties

Tanaka, Shinji,Suzuki, Yusuke,Kimura, Takahiro,Kitamura, Masato

, p. 1707 - 1720 (2019/10/01)

A CpRu/Br?nsted acid-combined catalyst, CpRu(II)/pico-linic acid (PyCOOH), acts as an efficient catalyst for the allyl protection/deprotection of alcohols. This discovery has resulted in the development of a new axially chiral ligand, Cl-Naph-PyCOOH (2a;

Antiallergic agents. 2. N-(1H-tetrazol-5-yl)-6-phenyl-2-pyridinecarboxamides

Honma,Oda,Hashiyama,Hanamoto,Nakai,Inoue,Ishida,Takeda,Ono,Tsuzurahara

, p. 1499 - 1504 (2007/10/02)

A new series of N-(1H-tetrazol-5-yl)-6-phenyl-2-pyridinecarboxamides was prepared to determine the effects of substituents on the benzene and pyridine rings on antiallergic activity in the rat passive cutaneous anaphylaxis (PCA) assay after oral administr

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