5831-77-6 Usage
Description
2-Allyloxypyridine is a colorless to light yellow liquid with a pungent odor, belonging to the class of organic compounds known as pyridines. It features a pyridine ring with an allyloxy group attached, which imparts its characteristic properties. This chemical compound is considered hazardous and should be handled with care to avoid skin and eye irritation, as well as respiratory and digestive issues from ingestion or inhalation.
Uses
Used in Flavor and Fragrance Industry:
2-Allyloxypyridine is used as a flavoring agent and fragrance ingredient in the food and cosmetic industries, providing unique scents and enhancing the sensory experience of products.
Used in Pharmaceutical and Agrochemical Synthesis:
It serves as a building block in the synthesis of various pharmaceuticals and agrochemicals, contributing to the development of new drugs and agricultural products that can improve health and crop protection.
Check Digit Verification of cas no
The CAS Registry Mumber 5831-77-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5831-77:
(6*5)+(5*8)+(4*3)+(3*1)+(2*7)+(1*7)=106
106 % 10 = 6
So 5831-77-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H9NO/c1-2-7-10-8-5-3-4-6-9-8/h2-6H,1,7H2
5831-77-6Relevant articles and documents
In situ synthesis of 2-allyloxy-1-methylpyridinium triflate for the allylation of carboxylic acids
Strayer, Timothy A.,Culy, Caleb C.,Bunner, Matthew H.,Frank, Amie R.,Albiniak, Philip A.
supporting information, p. 6807 - 6809 (2016/01/26)
2-Allyloxypyridinium triflate is formed in situ by treating a mixture of 2-allyloxypyridine, a carboxylic acid, and toluene with methyl triflate. Subsequent warming of the reaction mixture in the presence of potassium carbonate leads to efficient formation of allyl esters in good to excellent yields.
Indium-mediated deoxygenation of amine-N-oxides in aqueous media
Yadav,Subba Reddy,Reddy, M. Muralidhar
, p. 2663 - 2665 (2007/10/03)
Several aromatic and aliphatic amine-N-oxides were deoxygenated to the corresponding amines in good to quantitative yield using indium metal in neutral aqueous media. Other functional groups such as alkenes, halides, esters, ethers, nitriles, amides and sulfones are unaffected under the present reaction conditions. (C) 2000 Elsevier Science Ltd.
