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5-Isocyano-2-methoxyphenol is an organic compound with the chemical formula C8H7NO2. It is characterized by the presence of an isocyano group (-CN) at the 5-position and a methoxy group (-OCH3) at the 2-position on a phenol ring. 5-isocyano-2-methoxyphenol is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical structure. It is a colorless to pale yellow solid and is sensitive to light and moisture, requiring proper storage conditions to maintain its stability. The compound's properties make it a valuable intermediate in the chemical industry, particularly for the production of compounds with biological activity.

1268445-45-9

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1268445-45-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268445-45-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,4,4 and 5 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1268445-45:
(9*1)+(8*2)+(7*6)+(6*8)+(5*4)+(4*4)+(3*5)+(2*4)+(1*5)=179
179 % 10 = 9
So 1268445-45-9 is a valid CAS Registry Number.

1268445-45-9Relevant academic research and scientific papers

A practical synthesis of 5-aroyl-1-aryltetrazoles using an Ugi-like 4-component reaction followed by a biomimetic transamination

Giustiniano, Mariateresa,Pirali, Tracey,Massarotti, Alberto,Biletta, Beatrice,Novellino, Ettore,Campiglia, Pietro,Sorba, Giovanni,Tron, Gian Cesare

experimental part, p. 4107 - 4118 (2011/03/17)

Multicomponent reactions (MCRs), followed by subsequent transformations, are fascinating tools for the rapid and effective synthesis of molecular scaffolds with potential pharmacological relevance. We became interested in the preparation of novel 5-aroyl-1-aryltetrazoles as (1) they still represent challenging structures not easily accessible through the methods described in literature, and (2) the -ketotetrazolic framework may be considered as a potential bioisostere of the enonic linker of chalcones. In the present work, a novel, simple, effective and general synthesis for this class of compounds is described. Georg Thieme Verlag Stuttgart - New York.

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