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67029-84-9

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67029-84-9 Usage

Description

6-Chloro-7-methylchromone, a chromone derivative with the molecular formula C11H7ClO2, features a chlorine atom at the 6 position and a methyl group at the 7 position. This chemical compound has garnered attention for its potential pharmaceutical and biological activities, such as anti-inflammatory, antioxidant, and antimicrobial properties. Additionally, it has been explored for its role in cancer research and as a potential drug candidate for a variety of medical conditions, making it a versatile and significant compound in the realm of research and development.

Uses

Used in Pharmaceutical Research:
6-Chloro-7-methylchromone is utilized as a pharmaceutical candidate for its anti-inflammatory properties, offering potential benefits in the treatment of inflammatory conditions by reducing inflammation and associated symptoms.
Used in Antioxidant Applications:
As an antioxidant, 6-CHLORO-7-METHYLCHROMONE is employed to combat oxidative stress and protect cells from damage caused by reactive oxygen species, which can contribute to various diseases and aging processes.
Used in Antimicrobial Research:
6-CHLORO-7-METHYLCHROMONE is used as an antimicrobial agent, demonstrating potential in fighting against microbial infections by inhibiting the growth of bacteria, fungi, or other microorganisms.
Used in Cancer Research:
In the field of cancer research, 6-CHLORO-7-METHYLCHROMONE is used as a potential drug candidate for its possible role in targeting cancer cells, with the aim of developing new therapeutic strategies for cancer treatment.
Used in Medical Condition Treatment:
6-CHLORO-7-METHYLCHROMONE is explored for its potential use in treating various medical conditions, leveraging its multifaceted biological activities to address a range of health issues.

Check Digit Verification of cas no

The CAS Registry Mumber 67029-84-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,2 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67029-84:
(7*6)+(6*7)+(5*0)+(4*2)+(3*9)+(2*8)+(1*4)=139
139 % 10 = 9
So 67029-84-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H9ClO2/c1-6-4-10-7(5-8(6)11)9(12)2-3-13-10/h4-5H,2-3H2,1H3

67029-84-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H26997)  6-Chloro-7-methylchromone, 98%   

  • 67029-84-9

  • 1g

  • 1118.0CNY

  • Detail
  • Alfa Aesar

  • (H26997)  6-Chloro-7-methylchromone, 98%   

  • 67029-84-9

  • 5g

  • 3875.0CNY

  • Detail

67029-84-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLORO-7-METHYLCHROMONE

1.2 Other means of identification

Product number -
Other names 4H-1-Benzopyran-4-one,6-chloro-7-Methyl

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:67029-84-9 SDS

67029-84-9Relevant articles and documents

Substituent-Oriented Synthesis of Substituted Pyrazoles/Chromeno[3,2- c]pyrazoles via Sequential Reactions of Chromones/3-Chlorochromones and Tosylhydrazones

Dai, Tianzi,Li, Qunyi,Zhang, Xiaofei,Yang, Chunhao

, p. 5913 - 5921 (2019/05/10)

A facile and efficient synthetic strategy for the chemoselective synthesis of monocyclic/tricyclic-fused pyrazoles was developed, and it was oriented by different 3-position substituents (H or Cl) on the chromones. The reaction proceeded in a one-pot sequential way with a broad substrate scope and moderate to excellent yields.

2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines

Iaroshenko, Viktor O.,Mkrtchyan, Satenik,Gevorgyan, Ashot,Miliutina, Mariia,Villinger, Alexander,Volochnyuk, Dmytro,Sosnovskikh, Vyacheslav Ya.,Langer, Peter

supporting information; experimental part, p. 890 - 894 (2012/02/02)

A divergent and regioselective approach to fused pyridines was developed through formal [3 + 3] cyclocondensations from simple 2,3-unsubstituted chromones or their enaminone precursors.

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