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5831-77-6

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5831-77-6 Usage

General Description

2-Allyloxypyridine is a chemical compound that belongs to the class of organic compounds known as pyridines. It is a colorless to light yellow liquid with a pungent odor, and it is commonly used as a flavoring agent and fragrance ingredient in the food and cosmetic industries. It is also used as a building block in the synthesis of various pharmaceuticals and agrochemicals. Its molecular structure consists of a pyridine ring with an allyloxy group attached to it, giving it its characteristic properties. 2-Allyloxypyridine is considered to be a hazardous chemical and should be handled with caution due to its potential to cause skin and eye irritation, as well as respiratory and digestive issues if ingested or inhaled.

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

5831-77-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enoxypyridine

1.2 Other means of identification

Product number -
Other names 2-Allyloxy-pyridin

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5831-77-6 SDS

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.

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