Welcome to LookChem.com Sign In|Join Free
  • or
2-Bromo-8-methylquinoline, a brominated derivative of quinoline, is an aromatic heterocyclic compound with the molecular formula C10H8BrN. It is a pale yellow solid that is insoluble in water but soluble in organic solvents. Known for its versatile reactivity, 2-Bromo-8-methylquinoline serves as a valuable building block in organic synthesis and pharmaceutical research, enabling the formation of a variety of other useful compounds.

99073-81-1

Post Buying Request

99073-81-1 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

99073-81-1 Usage

Uses

Used in Pharmaceutical Research and Development:
2-Bromo-8-methylquinoline is utilized as a precursor in the production of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications. Its unique chemical structure allows for the synthesis of various compounds with different biological activities.
Used in Agrochemical Production:
In the agrochemical industry, 2-Bromo-8-methylquinoline is employed as a starting material for the synthesis of agrochemicals, such as pesticides and herbicides. Its reactivity and ability to form diverse compounds make it a valuable component in the creation of effective and targeted agrochemical products.
Used in Dye Manufacturing:
2-Bromo-8-methylquinoline is also used in the production of dyes, where its chemical properties contribute to the creation of a wide range of colorants for various applications, including textiles, plastics, and printing inks.
Used in Academic Research:
In academic research settings, 2-Bromo-8-methylquinoline serves as a valuable compound for studying chemical reactions and exploring new synthetic pathways. Its versatility and reactivity make it an essential tool for researchers working in the fields of organic chemistry and medicinal chemistry.
Used in Industrial Applications:
Beyond its use in research and development, 2-Bromo-8-methylquinoline finds application in various industrial settings, where its unique properties are harnessed for the production of specialty chemicals and materials with specific functionalities.

Check Digit Verification of cas no

The CAS Registry Mumber 99073-81-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,0,7 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99073-81:
(7*9)+(6*9)+(5*0)+(4*7)+(3*3)+(2*8)+(1*1)=171
171 % 10 = 1
So 99073-81-1 is a valid CAS Registry Number.

99073-81-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-8-methylquinoline

1.2 Other means of identification

Product number -
Other names 2-Brom-8-methyl-chinolin

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:99073-81-1 SDS

99073-81-1Relevant academic research and scientific papers

A highly practical and convenient halogenation of fused heterocyclic N-oxides

Wang, Dong,Wang, Yuxi,Zhao, Junjie,Li, Linna,Miao, Longfei,Wang, Dong,Sun, Hua,Yu, Peng

, p. 5762 - 5768 (2016/08/30)

A novel, simple and practical method for the regioselective halogenation of fused heterocyclic N-oxides has been developed. It employs Vilsmeier reagent, generated in situ by POX3and DMF, as both the activating agent and the nucleophilic halide source. The method is amenable across a broad range of substrates, including quinolines, isoquinolines and the diazine N-oxides, possessing a variety of substitution patterns. Furthermore, all of the reagents associated are cheap and easy to obtain. The potential extension of this method to a one-pot oxidation/halogenation sequence that obviates the need for isolation of the N-oxide intermediates is also presented.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 99073-81-1