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2(1H)-Quinolinone, 6-hydroxy-1-methyl-5-(2-propenyl)- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

314770-67-7

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314770-67-7 Usage

Derivative of quinolinone

The compound is based on the core structure of quinolinone, which is a heterocyclic aromatic compound.

Contains a hydroxyl group

The compound has a -OH group, which is a functional group consisting of an oxygen atom bonded to a hydrogen atom.

Contains a methyl group

The compound has a -CH3 group, which is a functional group consisting of a carbon atom bonded to three hydrogen atoms.

Contains a propenyl group

The compound has a -CH=CH2 group, which is a functional group consisting of a carbon-carbon double bond and a hydrogen atom.

Used in the pharmaceutical industry

The compound is used as a building block for the synthesis of various drugs and pharmacologically active compounds.

Potential therapeutic properties

The compound has been studied for its potential anti-inflammatory and neuromodulatory effects.

Valuable tool for research and development

The unique structure and properties of the compound make it useful for research and development in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 314770-67-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,4,7,7 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 314770-67:
(8*3)+(7*1)+(6*4)+(5*7)+(4*7)+(3*0)+(2*6)+(1*7)=137
137 % 10 = 7
So 314770-67-7 is a valid CAS Registry Number.

314770-67-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-hydroxy-1-methyl-5-(prop-2-enyl)-quinolin-2(1H)-one

1.2 Other means of identification

Product number -
Other names 5-allyl-6-hydroxy-N-methylquinolin-2-one

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:314770-67-7 SDS

314770-67-7Relevant academic research and scientific papers

Regioselective synthesis of pyrano[3,2-f]quinolin-2(7H)-ones and Furo[3,2-f]quinolin-2-ones

Majumdar, Krishna C.,Ghosh, Safalla K.,Biswas, Paritosh

, p. 967 - 973 (2000)

A simple and efficient synthesis of the hitherto unreported ring systems pyrano[3,2-f]quinolin-2(7H)-one and furo[3,2-f]quinolin-2-one was accomplished via a thermal [3,3]-sigmatropic rearrangement.

Sequential Claisen rearrangement and intramolecular Heck reaction as a route to medium-ring oxacycle-fused heterocycles

Chattopadhyay, Shital K.,Neogi, Kaushik,Singha, Sovan K.,Dey, Rajat

scheme or table, p. 1137 - 1140 (2009/04/05)

A synthetic strategy based on tandem application of Claisen rearrangement and intramolecular Heck reaction as key steps has been developed for the synthesis of various hitherto unknown benzoxocine- and benzoxonine-fused coumarin and quinolone derivatives.

Regioselective synthesis of oxepin- and oxocin-annulated 2-quinolones

Chattopadhyay, Shital K.,Dey, Rajat,Biswas, Suman

, p. 403 - 406 (2007/10/03)

A synthetic strategy based on tandem Claisen rearrangement and ring-closing metathesis was developed for the regioselective synthesis of some hitherto unknown oxepin- and oxocin-annulated 2-quinolones. Georg Thieme Verlag Stuttgart.

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