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4-Pyridylmethyl N-phenylcarbamate is a chemical compound with the molecular formula C13H12N2O2. It is a derivative of phenylcarbamic acid, featuring a pyridine ring attached to the carbamate group. 4-pyridylmethyl N-phenylcarbamate is known for its potential applications in pharmaceuticals and agrochemicals, particularly as a precursor in the synthesis of various biologically active molecules. It is characterized by its white crystalline appearance and is typically used in research and development settings due to its reactivity and structural properties. The compound's specific role in chemical synthesis and its potential impact on drug discovery make it a significant entity in the field of organic chemistry.

6457-74-5

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6457-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6457-74-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,5 and 7 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6457-74:
(6*6)+(5*4)+(4*5)+(3*7)+(2*7)+(1*4)=115
115 % 10 = 5
So 6457-74-5 is a valid CAS Registry Number.

6457-74-5Downstream Products

6457-74-5Relevant academic research and scientific papers

NEW PYRIDINE DERIVATIVES AS LEPTIN RECEPTOR MODULATOR MIMETICS

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Page/Page column 29-30, (2009/12/28)

The present invention relates to new compounds of formula (I), to pharmaceutical compositions comprising these compounds and to the use of these compounds as leptin receptor modulator mimetics in the preparation of medicaments against conditions associated with weight gain, type 2 diabetes and dyslipidemias.

The Pyridine-catalysed Reaction of Methanol with Phenyl Isocyanate in Tetrachloromethane

Moodie, Roy B.,Sansom, Peter J.

, p. 664 - 669 (2007/10/02)

The title reaction is first order in catalyst and each reactant.Several 3- and 4-substituted pyridine catalysts generate a Broensted plot with slope β of 0.49.This, the steric effect of 2,4,6-trimethylpyridine, the deuterium isotope effect, and the solvent effect are consistent with the general base mechanism of catalysis.The nucleophilic mechanism is considered relatively unlikely. 2-Pyridylmethanol reacts with phenyl isocyanate faster than does 4-pyridilmethanol, indicating intramolecular general base catalysis in the former case.

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