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Benzamide, 3,4,5-trimethoxy-N-2-pyridinyl-, also known as 2-(3,4,5-trimethoxybenzamido)pyridine, is a chemical compound with the molecular formula C15H16N2O5. It is a derivative of benzamide, featuring a pyridine ring attached to the amide group, and three methoxy groups (-OCH3) substituting the 3rd, 4th, and 5th positions of the benzene ring. Benzamide, 3,4,5-trimethoxy-N-2-pyridinyl- is characterized by its white crystalline appearance and is soluble in organic solvents. It has potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and properties.

4997-88-0

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4997-88-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4997-88-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,9 and 7 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 4997-88:
(6*4)+(5*9)+(4*9)+(3*7)+(2*8)+(1*8)=150
150 % 10 = 0
So 4997-88-0 is a valid CAS Registry Number.

4997-88-0Downstream Products

4997-88-0Relevant academic research and scientific papers

Optimization of Synthetically Versatile Pyridylidene Amide Ligands for Efficient Iridium-Catalyzed Water Oxidation

Navarro, Miquel,Smith, Christene A.,Li, Mo,Bernhard, Stefan,Albrecht, Martin

, p. 6386 - 6398 (2018/04/30)

The synthetic versatility of pyridylidene amide (PYA) ligands has been exploited to prepare and evaluate a diverging series of iridium complexes containing C,N-bidentate chelating aryl-PYA ligands for water oxidation catalysis. The phenyl-PYA lead structu

Copper-catalyzed highly efficient oxidative amidation of aldehydes with 2-aminopyridines in an aqueous micellar system

Patel, Om P. S.,Anand, Devireddy,Maurya, Rahul K.,Yadav, Prem P.

supporting information, p. 3728 - 3732 (2015/07/15)

An environmentally benign protocol for the synthesis of N-(pyridine-2-yl)amides from aldehydes and 2-aminopyridines has been developed under mild reaction conditions. This approach requires Cu(OTf)2 as a catalyst, and inexpensive molecular iodi

Synthesis and CNS-depressant profile of 3,4,5-trimethoxybenzoyl analogues

Kar

, p. 313 - 315 (2007/10/02)

A series of 3,4,5-trimethoxybenzoyl analogues with varying electronic and stereochemical characteristics has been synthesized. Many of these compounds (4, 5, 9, 12, 15) showed appreciable potentiation of pentobarbitone-induced hypnosis. Several analogues (1, 5, 6, 11, 12, 15) exhibited marked reduction of spontaneous motor activity (SMA).

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