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2683-35-4

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2683-35-4 Usage

General Description

3,5-DibroMo-1-Methylpyridin-4(1H)-one, also known as N-methyl-3,5-dibromo-4-pyridone, is a chemical compound with the molecular formula C6H5Br2NO. It is a white to off-white crystalline solid with a melting point of 146-150°C. 3,5-DibroMo-1-Methylpyridin-4(1H)-one is commonly used in the synthesis of pharmaceuticals and agrochemicals and can also act as a building block in organic synthesis. Additionally, it can be utilized in the preparation of enantiomerically pure compounds. Its chemical structure and properties make it a versatile and valuable reagent in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 2683-35-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,8 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2683-35:
(6*2)+(5*6)+(4*8)+(3*3)+(2*3)+(1*5)=94
94 % 10 = 4
So 2683-35-4 is a valid CAS Registry Number.

2683-35-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dibromo-1-methylpyridin-4-one

1.2 Other means of identification

Product number -
Other names 3,5-Dibrom-1-methyl-pyridon-4

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:2683-35-4 SDS

2683-35-4Relevant articles and documents

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Beak,Bonham

, p. 3365,3368 (1965)

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Kinetics and mechanism of the bromination of 4-pyridone and related derivatives in aqueous solution

Tee, Oswald S.,Paventi, Martino

, p. 2556 - 2562 (2007/10/02)

The kinetics of bromination of 4-pyridone and selected derivatives have been measured in aqueous solutions in the pH range 0-9, at 25 deg C.The tautomeric system 4-pyridone 4-hydroxypyridine (1a 2a) reacts with bromine via the predominant (pyridone) tautomer at pH 6. 3-Bromo-4-pyridone behaves similary.The kinetics also reveal that the facile dibromination of 4-pyridone occurs because at most pH's the monobromo derivative is actually more reactive towards bromine by virtue of its lower pKa values.From the point of view of reactivity the 4-pyridones and their anions behave as substituted phenoxide ions. 4-Methoxypyridine does not undergo bromination under comparable conditions, but rather forms a complex with bromine.

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