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115237-39-3

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115237-39-3 Usage

General Description

3,6-dibromochromone is a chemical compound with the molecular formula C10H4Br2O2. It belongs to the class of organic compounds known as flavonoids, which are natural substances found in fruits and vegetables and are known for their antioxidant and anti-inflammatory properties. 3,6-dibromochromone is a derivative of chromone, a heterocyclic compound containing a benzopyrone core. It is used in the field of medicinal chemistry and pharmacology for its potential pharmaceutical applications, including its antioxidant, anti-inflammatory, and anticancer properties. The compound has been studied for its potential to inhibit the growth of cancer cells and to protect against oxidative stress and inflammation in the body.

Check Digit Verification of cas no

The CAS Registry Mumber 115237-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,2,3 and 7 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 115237-39:
(8*1)+(7*1)+(6*5)+(5*2)+(4*3)+(3*7)+(2*3)+(1*9)=103
103 % 10 = 3
So 115237-39-3 is a valid CAS Registry Number.

115237-39-3SDS

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 3,6-dibromochromone

1.2 Other means of identification

Product number -
Other names 3,6-dibromo-4H-1-benzopyran-4-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:115237-39-3 SDS

115237-39-3Relevant articles and documents

Electrochemical C-H Halogenations of Enaminones and Electron-Rich Arenes with Sodium Halide (NaX) as Halogen Source for the Synthesis of 3-Halochromones and Haloarenes

Jin, Jun,Lin, Yan,Liu, Yunyun,Wan, Jie-Ping,Wang, Chaoli

, p. 12378 - 12385 (2021/09/07)

Without employing an external oxidant, the simple synthesis of 3-halochromones and various halogenated electron-rich arenes has been realized with electrode oxidation by employing the simplest sodium halide (NaX, X = Cl, Br, I) as halogen source. This electrochemical method is advantageous for the simple and mild room temperature operation, environmental friendliness as well as broad substrate scope in both C-H bond donor and halogen source components.

Substituted 4H-1-Benzopyran-4-ones (Chromones): Synthesis via Palladium-catalysed Coupling of their Halogeno Derivatives with Alkenes

Davies, Stephen G.,Mobbs, Bryan E.,Goodwin, Christopher J.

, p. 2597 - 2604 (2007/10/02)

Activation of bromochromones has been achieved by Pd0 insertion into the carbon-halogen bond.The resultant species undergo coupling with alkenes leading to vinylated chromones.Vinylation occurs regiospecifically at the original site of bromination and therefore provides a method for the clean introduction of substituents into the chromone ring system.An anomalous reaction of a dibrominated chromone leading to a ring-opened product is described.

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