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Quinoline, 4-(bromomethyl)-2-methyl-, also known as 2-Methyl-4-(bromomethyl)quinoline, is a chemical compound with the molecular formula C10H10BrN. It is a derivative of quinoline, featuring a bromomethyl group at the 4th position and a methyl group at the 2nd position. Quinoline, 4-(bromomethyl)-2-methylis known for its potential applications in various fields, including pharmaceuticals, dyes, and agrochemicals, due to its unique structural properties and functional groups.

864779-06-6

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864779-06-6 Usage

Uses

Used in Pharmaceutical Synthesis:
Quinoline, 4-(bromomethyl)-2-methylis utilized as an intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, such as antimicrobial, antifungal, and anticancer agents.
Used in Dye Production:
Quinoline, 4-(bromomethyl)-2-methylis also used in the production of dyes, where its chemical properties contribute to the color and stability of the dyes. Its versatility in chemical reactions enables the creation of a wide range of dyes for various applications, including textiles, plastics, and printing inks.
Used in Agrochemical Development:
Quinoline, 4-(bromomethyl)-2-methylis employed in the development of agrochemicals, particularly as a precursor for the synthesis of pesticides and fungicides. Its antimicrobial and antifungal properties make it a valuable component in the creation of effective crop protection products.
Used in Organic Synthesis:
As a precursor in the synthesis of various organic compounds, Quinoline, 4-(bromomethyl)-2-methylis used in research and industrial applications. Its ability to participate in a range of chemical reactions, such as nucleophilic substitution and electrophilic aromatic substitution, makes it a versatile building block for the synthesis of complex organic molecules.
Used in Research Applications:
In the field of research, Quinoline, 4-(bromomethyl)-2-methylis used to study the properties and reactions of quinoline derivatives. Its unique structure provides insights into the reactivity and selectivity of various chemical transformations, contributing to the advancement of organic chemistry and related disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 864779-06-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,7,7 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 864779-06:
(8*8)+(7*6)+(6*4)+(5*7)+(4*7)+(3*9)+(2*0)+(1*6)=226
226 % 10 = 6
So 864779-06-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H10BrN/c1-8-6-9(7-12)10-4-2-3-5-11(10)13-8/h2-6H,7H2,1H3

864779-06-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Bromomethyl)-2-methylquinoline

1.2 Other means of identification

Product number -
Other names 2-methyl-4-bromomethyl quinoline

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:864779-06-6 SDS

864779-06-6Downstream Products

864779-06-6Relevant articles and documents

Substituted Heterocyclic Ethers and Their Use in CNS Disorders

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Page/Page column 20, (2009/01/24)

The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts, their pharmaceutical compositions, and their use in treating CNS disorders.

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