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N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide is a chemical compound characterized by the molecular formula C13H18N2O2. It is a propionamide derivative featuring a methoxy-pyridinyl group and two methyl substituents on the propionamide moiety. N-(6-METHOXY-PYRIDIN-2-YL)-2,2-DIMETHYLPROPIONAMIDE is recognized for its unique chemical and biological properties, which render it a valuable building block in the development of pharmaceuticals for diverse applications.

851102-40-4

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851102-40-4 Usage

Uses

Used in Organic Synthesis:
N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide is utilized as a key intermediate in organic synthesis, contributing to the formation of complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a wide range of compounds.
Used in Pharmaceutical Research:
In the pharmaceutical industry, N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide serves as a building block for the development of innovative drug molecules. Its specific chemical properties make it an essential component in the design and synthesis of new pharmaceuticals aimed at treating various medical conditions.
Used in Drug Development:
N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide is employed in drug development to create novel therapeutic agents. Its incorporation into drug molecules can potentially enhance their efficacy, selectivity, and pharmacokinetic properties, leading to improved treatments for patients.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide is used for the study of its biological activities and interactions with biological targets. Understanding its mode of action can aid in the discovery of new drugs with optimized pharmacological profiles.
Overall, N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide is a versatile chemical compound with significant applications in various scientific and industrial fields, particularly in the development of new pharmaceuticals for improved healthcare solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 851102-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,1,0 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 851102-40:
(8*8)+(7*5)+(6*1)+(5*1)+(4*0)+(3*2)+(2*4)+(1*0)=124
124 % 10 = 4
So 851102-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C11H16N2O2/c1-11(2,3)10(14)13-8-6-5-7-9(12-8)15-4/h5-7H,1-4H3,(H,12,13,14)

851102-40-4 Well-known Company Product Price

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  • Aldrich

  • (ADE000330)  N-(6-Methoxy-pyridin-2-yl)-2,2-dimethylpropionamide  AldrichCPR

  • 851102-40-4

  • ADE000330-1G

  • 4,512.69CNY

  • Detail

851102-40-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(6-methoxypyridin-2-yl)-2,2-dimethylpropanamide

1.2 Other means of identification

Product number -
Other names -

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

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More Details:851102-40-4 SDS

851102-40-4Relevant academic research and scientific papers

Rhodium(III)-catalyzed oxidative olefination of pyridines and quinolines: Multigram-scale synthesis of naphthyridinones

Zhou, Jun,Li, Bo,Hu, Fang,Shi, Bing-Feng

supporting information, p. 3460 - 3463 (2013/07/26)

A Rh(III)-catalyzed oxidative olefination of pyridines and quinolines has been achieved. This method has a broad substrate scope and has been applied to the expeditious, multigram-scale synthesis of naphthyridinones.

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