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85344-72-5

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85344-72-5 Usage

Description

N-(2-methoxyphenyl)picolinamide, also known as N-methoxy-2-picolinamide, is a chemical compound with the molecular formula C12H11N3O2. It is a derivative of picolinamide, a type of amide derived from picolinic acid. N-(2-methoxyphenyl)picolinamide features a picolinamide core with a methoxyphenyl group attached to the amino nitrogen, endowing it with unique chemical properties and reactivity.

Uses

Used in Pharmaceutical Research:
N-(2-methoxyphenyl)picolinamide is utilized as a reagent in pharmaceutical research for the development of new drug molecules. Its unique structure and reactivity make it a valuable component in the synthesis of potential therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, N-(2-methoxyphenyl)picolinamide serves as a key intermediate, facilitating the creation of various complex organic compounds for a range of applications.
Used in Agriculture:
N-(2-methoxyphenyl)picolinamide has potential applications in agriculture, possibly as a component in the development of agrochemicals or as a tool in the study of plant-pest interactions.
Used in Material Science:
Its unique chemical properties also lend N-(2-methoxyphenyl)picolinamide potential uses in material science, where it could contribute to the advancement of new materials with specific properties for various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 85344-72-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,4 and 4 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85344-72:
(7*8)+(6*5)+(5*3)+(4*4)+(3*4)+(2*7)+(1*2)=145
145 % 10 = 5
So 85344-72-5 is a valid CAS Registry Number.

85344-72-5SDS

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 N-(2-Methoxyphenyl)-2-pyridinecarboxamide

1.2 Other means of identification

Product number -
Other names Pyridin-2-carbonsaeure-o-anisidid

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:85344-72-5 SDS

85344-72-5Relevant articles and documents

Enantioselective Synthesis of Atropisomeric Anilides via Pd(II)-Catalyzed Asymmetric C-H Olefination

Yao, Qi-Jun,Xie, Pei-Pei,Wu, Yong-Jie,Feng, Ya-Lan,Teng, Ming-Ya,Hong, Xin,Shi, Bing-Feng

supporting information, p. 18266 - 18276 (2020/11/02)

Atropisomeric anilides have received tremendous attention as a novel class of chiral compounds possessing restricted rotation around an N-aryl chiral axis. However, in sharp contrast to the well-studied synthesis of biaryl atropisomers, the catalytic asym

Copper-Catalyzed C-4 Carboxylation of 1-Naphthylamide Derivatives with CBr4/MeOH

Sahoo, Tapan,Sen, Chiranjit,Singh, Harshvardhan,Suresh,Ghosh, Subhash Chandra

supporting information, p. 3950 - 3957 (2019/07/19)

A simple and practical copper catalyzed C-4 carboxylation reaction of 1-naphthylamide derivatives using carbon tetra bromide and methanol is reported here. Picolinamide and its derivatives are used as a bidentate directing group for the distal C4-H functi

Proteomimetic compounds and methods

-

, (2008/06/13)

The present invention relates to compounds and pharmaceutical compositions which are proteomimetic and to methods for inhibiting the interaction of an alpha-helical protein with another protein or binding site. Methods for treating diseases or conditions which are modulated through interactions between alpha helical proteins and their binding sites are other aspects of the invention.

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