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136117-46-9

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136117-46-9 Usage

General Description

5-Acetyl-3-bromo-6-methyl-2(1H)-pyridinone is a chemical compound known for its use in pharmaceutical research and drug development. It is a pyridinone derivative with a bromine and acetyl group attached to the 3 and 5 positions of the pyridinone ring, and a methyl group at the 6 position. 5-Acetyl-3-bromo-6-methyl-2(1H)-pyridinone has displayed potential biological activities, including antiviral, antimicrobial, and antitumor properties. It has been studied for its potential as a therapeutic agent for a range of diseases. 5-Acetyl-3-bromo-6-methyl-2(1H)-pyridinone's structure and properties make it an interesting and promising target for further research in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 136117-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,1,1 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 136117-46:
(8*1)+(7*3)+(6*6)+(5*1)+(4*1)+(3*7)+(2*4)+(1*6)=109
109 % 10 = 9
So 136117-46-9 is a valid CAS Registry Number.

136117-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-acetyl-3-bromo-6-methyl-1H-pyridin-2-one

1.2 Other means of identification

Product number -
Other names 5-acetyl-3-bromo-6-methyl-2(1H)-pyridinone

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:136117-46-9 SDS

136117-46-9Relevant articles and documents

AN EFFICIENT AND NOVEL SYNTHESIS OF FUSED THIAZOL-2(3H)-ONES

Singh, Baldev,Pennock, Patrick O.,Lesher, George Y.,Bacon, Edward R.,Page, Donald F.

, p. 133 - 144 (2007/10/02)

Reaction of o-bromo aromatic amines (2, 4, 7, 10, 15) with ethyl potassium xanthate gave the corresponding fused thiazol-2(3H)-thiones (16, 19, 22) which in turn were first alkylated with methyl iodide and then treated with sodium methoxide to produce fus

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