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7-Bromo-2,8-dimethylquinoline is a quinoline-based heterocyclic compound that features a nitrogen-containing aromatic structure. It is characterized by the presence of a bromine atom at the 7th position and two methyl groups at the 2nd and 8th positions. 7-Bromo-2,8-dimethylquinoline has been recognized for its potential in medicinal chemistry, particularly in drug discovery and development. Its distinctive structure and reactivity contribute to its value as a building block for synthesizing biologically active molecules, with promising applications in the creation of new pharmaceuticals. Furthermore, it may also find use in fields like materials science and organic synthesis.

1189106-33-9

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1189106-33-9 Usage

Uses

Used in Pharmaceutical Industry:
7-Bromo-2,8-dimethylquinoline is utilized as a key intermediate in the synthesis of various biologically active molecules. Its unique structure allows it to be a valuable component in the development of new pharmaceuticals, contributing to drug discovery and innovation.
Used in Medicinal Chemistry:
As a building block in medicinal chemistry, 7-Bromo-2,8-dimethylquinoline is employed for its potential to create compounds with specific therapeutic properties. Its reactivity and structural features make it suitable for the design and synthesis of molecules targeting various medical conditions.
Used in Drug Discovery:
7-Bromo-2,8-dimethylquinoline plays a role in drug discovery as a starting material for the development of novel pharmaceutical agents. Its unique attributes can be leveraged to create new drugs with improved efficacy and selectivity.
Used in Materials Science:
Although not explicitly mentioned in the provided materials, the compound's potential applications in materials science could be explored due to its structural properties. It may contribute to the development of new materials with specific characteristics for various industrial applications.
Used in Organic Synthesis:
7-Bromo-2,8-dimethylquinoline is used as a reactant in organic synthesis processes. Its reactivity and the presence of functional groups make it a candidate for creating a range of organic compounds for different purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 1189106-33-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,1,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1189106-33:
(9*1)+(8*1)+(7*8)+(6*9)+(5*1)+(4*0)+(3*6)+(2*3)+(1*3)=159
159 % 10 = 9
So 1189106-33-9 is a valid CAS Registry Number.

1189106-33-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-Bromo-2,8-dimethylquinoline

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1189106-33-9 SDS

1189106-33-9Downstream Products

1189106-33-9Relevant academic research and scientific papers

Synthesis of substituted 2-alkylquinolines by visible-light photoredox catalysis

Mei, Yousheng,Liu, Jie,Wang, Lei,Li, Pinhua

supporting information, p. 86 - 92 (2019/12/26)

The condensation of anilines and alkenyl ethers has been demonstrated by employing visible-light photoredox catalysis. The resulting method enables the synthesis of substituted 2-alkylquinolines under mild and simple conditions with good substrate scope and high yields.

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