Welcome to LookChem.com Sign In|Join Free

CAS

  • or
2-Bromo-6-methylquinoline is a heterocyclic compound with the molecular formula C10H8BrN. It is a substituted quinoline derivative that features a bromine atom and a methyl group attached to the quinoline ring. Known for its versatile chemical properties, 2-Bromo-6-methylquinoline plays a significant role in the field of organic chemistry, particularly as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and as a building block in organic synthesis reactions.

302939-86-2

Post Buying Request

302939-86-2 Suppliers

Recommended suppliersmore

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

302939-86-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-6-methylquinoline is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into complex molecular structures, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Bromo-6-methylquinoline serves as an intermediate in the production of agrochemicals, such as pesticides and herbicides, due to its reactivity and capacity to form stable compounds with biological activity.
Used in Organic Synthesis:
2-Bromo-6-methylquinoline is utilized as a building block in organic synthesis reactions, allowing for the creation of a wide range of organic compounds with diverse applications across various industries, including the development of new materials and chemical products.

Check Digit Verification of cas no

The CAS Registry Mumber 302939-86-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,2,9,3 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 302939-86:
(8*3)+(7*0)+(6*2)+(5*9)+(4*3)+(3*9)+(2*8)+(1*6)=142
142 % 10 = 2
So 302939-86-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrN/c1-7-2-4-9-8(6-7)3-5-10(11)12-9/h2-6H,1H3

302939-86-2SDS

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 2-Bromo-6-methylquinoline

1.2 Other means of identification

Product number -
Other names Quinoline,2-bromo-6-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:302939-86-2 SDS

302939-86-2Downstream Products

302939-86-2Relevant articles and documents

Structure-based design and profiling of novel 17β-HSD14 inhibitors

Braun, Florian,Bertoletti, Nicole,M?ller, Gabriele,Adamski, Jerzy,Frotscher, Martin,Guragossian, Nathalie,Madeira Gírio, Patrícia Alexandra,Le Borgne, Marc,Ettouati, Laurent,Falson, Pierre,Müller, Sebastian,Vollmer, Günther,Heine, Andreas,Klebe, Gerhard,Marchais-Oberwinkler, Sandrine

supporting information, p. 61 - 76 (2018/06/01)

The human enzyme 17β-hydroxysteroid dehydrogenase 14 (17β-HSD14) oxidizes the hydroxyl group at position 17 of estradiol and 5-androstenediol using NAD+ as cofactor. However, the physiological role of the enzyme remains unclear. We recently des

Quinoline derivatives and their use

-

Paragraph 0099-0101; 0168; 0169; 0186; 0187, (2017/03/14)

The invention discloses a quinoline derivative and a usage thereof, a compound with a structure as shown in a formula (I) and or a pharmaceutically acceptable salt of the compound. The compound or the pharmaceutically acceptable salt thereof disclosed by the invention can be applied to the field of preparation of drugs for preventing or treating tumors.

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.

Development of a facile and inexpensive route for the preparation of α-halobenzopyridines from α-unsubstituted benzopyridines

Sugimoto, Osamu,Iwasaki, Hyuma,Tanji, Ken-Ichi

, p. 1445 - 1454 (2015/07/15)

A facile and inexpensive route for the preparation of α-halobenzopyridines from α-unsubstituted benzopyridines via N-methylbenzopyridin-α-ones was developed. α-Unsubstituted benzopyridines were converted easily into the corresponding N-methylbenzopyridin-α-ones, which were halogenated using PPh3-TCICA or PPh3-DBICA without using solvent to give α-halobenzopyridines.

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

What can I do for you?
Get Best Price

Get Best Price for 302939-86-2