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6431-84-1

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6431-84-1 Usage

General Description

2(1H)-Quinolinone, 4-hydroxy-3-(3-methyl-2-butenyl)- is a chemical compound with the molecular formula C16H15NO2. It is a derivative of quinolinone and is also known as 4-hydroxy-3-prenylquinolin-2(1H)-one. 2(1H)-Quinolinone, 4-hydroxy-3-(3-methyl-2-butenyl)- has been studied for its potential biological and pharmacological properties, including its antioxidant and anti-inflammatory effects. It has also been investigated for its potential use in the development of new drugs for various medical conditions. Additionally, it has shown potential as a natural flavoring agent and is found in certain plant species. More research is needed to fully understand the potential uses and effects of 2(1H)-Quinolinone, 4-hydroxy-3-(3-methyl-2-butenyl)-.

Check Digit Verification of cas no

The CAS Registry Mumber 6431-84-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,3 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 6431-84:
(6*6)+(5*4)+(4*3)+(3*1)+(2*8)+(1*4)=91
91 % 10 = 1
So 6431-84-1 is a valid CAS Registry Number.

6431-84-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-hydroxy-3-(3-methylbut-2-enyl)-1H-quinolin-2-one

1.2 Other means of identification

Product number -
Other names -

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

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More Details:6431-84-1 SDS

6431-84-1Relevant articles and documents

A REVERSIBLE CLAISEN REARRANGEMENT OF 3-(3,3-DIMETHYLALLYL)-4-(3,3-DIMETHYLALLYLOXY)QUINOLIN-2-ONE; SYNTHESIS OF BUCHAPSINE AND LOSS OF ITS 1,1-DIMETHYLALLYL GROUP

Grundon, Michael F.,Ramachandran, V. N.

, p. 4253 - 4256 (2007/10/02)

Reversible Claisen rearrangement of 3-(3,3-dimethylallyl)-4-(3,3-dimethylallyloxy)quinolin-2-one (5) furnished the alkaloid, buchapsine (6), which readily lost the 1,1-dimethylallyl group; a mechanism for the cleavage reaction is proposed.

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