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(Anilino-pyridin-2-yl-methyl)-phosphonic acid diphenyl ester is a complex organic compound with the chemical formula C23H20NO3P. It is a derivative of phosphonic acid, featuring an anilino group attached to a pyridin-2-yl-methyl moiety. This molecule is characterized by its potential applications in medicinal chemistry, particularly as a precursor or intermediate in the synthesis of various pharmaceuticals. The diphenyl ester group enhances its reactivity and stability, making it a valuable building block in the development of new drugs. Its structure and properties make it a subject of interest for researchers in the field of organic and medicinal chemistry.

3360-70-1

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3360-70-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3360-70-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3360-70:
(6*3)+(5*3)+(4*6)+(3*0)+(2*7)+(1*0)=71
71 % 10 = 1
So 3360-70-1 is a valid CAS Registry Number.

3360-70-1Relevant academic research and scientific papers

Calcitonin gene-related peptide (CGRP) receptor antagonists: Pyridine as a replacement for a core amide group

Luo, Guanglin,Chen, Ling,Civiello, Rita,Pin, Sokhom S.,Xu, Cen,Kostich, Walter,Kelley, Michelle,Conway, Charles M.,MacOr, John E.,Dubowchik, Gene M.

scheme or table, p. 2917 - 2921 (2012/06/04)

In our continuing efforts to identify CGRP receptor antagonists that can be dosed orally for the treatment of migraine headache, we have investigated a pyridine bioisosteric replacement of a polar amide portion of a previous lead compound, BMS-694153. Pyr

4- (HETEROCYCLYL- FUSED PHENYL)- 3- (PHENYL OR PYRID -2- YL) PYRAZOLES AS INHIBITORS OF THE ALK-5- RECEPTOR

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Page 24, (2008/06/13)

The invention relates to novel pyrazole derivatives which are inhibitors of the transforming growth factor, ("TGF")-β signalling pathway, in particular, the phosphorylation of smad2 or smad3 by the TGF-β type I or activin-like kinase ("ALK")-5 receptor, m

An improved and practical procedure for the synthesis of substituted phenylacetylpyridines

Journet, Michel,Cai, Dongwei,Larsen, Robert D.,Reider, Paul J.

, p. 1717 - 1720 (2007/10/03)

A general procedure for the synthesis of substituted phenylacetylpyridines in excellent yields is described using a Horner-Emmons condensation between α-aminoalkylphosphonates of pyridinecarboxaldehydes and benzaldehydes with cesium carbonate at room temperature.

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