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948289-14-3

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948289-14-3 Usage

Description

6-BROMO-2-METHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is a chemical compound with the molecular formula C13H11BrN2O2, belonging to the quinoline family. It is a yellow crystalline powder that is sparingly soluble in water but soluble in organic solvents. Due to its potential to cause irritation to the skin, eyes, and respiratory system, careful handling is required.
Used in Pharmaceutical Industry:
6-BROMO-2-METHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is used as an intermediate for the synthesis of various drugs, contributing to the development of new pharmaceuticals.
Used in Agrochemical Industry:
6-BROMO-2-METHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a building block for the synthesis of agrochemicals, playing a role in the creation of products for agricultural applications.
Used in Research Chemicals:
6-BROMO-2-METHYLQUINOLINE-3-CARBOXYLIC ACID ETHYL ESTER is used as a research chemical, aiding scientists in their studies and experiments to advance knowledge in various chemical and biological fields.

Check Digit Verification of cas no

The CAS Registry Mumber 948289-14-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,8,2,8 and 9 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 948289-14:
(8*9)+(7*4)+(6*8)+(5*2)+(4*8)+(3*9)+(2*1)+(1*4)=223
223 % 10 = 3
So 948289-14-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12BrNO2/c1-3-17-13(16)11-7-9-6-10(14)4-5-12(9)15-8(11)2/h4-7H,3H2,1-2H3

948289-14-3 Well-known Company Product Price

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  • Aldrich

  • (BBO000199)  6-Bromo-2-methylquinoline-3-carboxylic acid ethyl ester  AldrichCPR

  • 948289-14-3

  • BBO000199-1G

  • 2,901.60CNY

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948289-14-3SDS

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 Ethyl 6-bromo-2-methylquinoline-3-carboxylate

1.2 Other means of identification

Product number -
Other names 6-Bromo-2-methylquinoline-3-carboxylic acid ethyl ester

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:948289-14-3 SDS

948289-14-3Relevant articles and documents

Lewis Acid-Catalyzed C(sp3)–C(sp3) Bond Forming Cyclization Reactions for the Synthesis of Tetrahydroprotoberberine Derivatives

Li, Jianjun,Qin, Cong,Yu, Yang,Fan, Huaqiang,Fu, Yiwei,Li, Hao,Wang, Wei

supporting information, p. 2191 - 2195 (2017/07/07)

An efficient Lewis acid-catalyzed C(sp3)–C(sp3) bond forming annulation reaction has been developed. This strategy serves as a new method for the facile synthesis of tetrahydro-5H-isoquinolino[2,1-g][1,6]naphthyridine derivatives. A wide range of 2-methylquinoline-3-carbaldehydes and 1,2,3,4-tetrahydroisoquinolines can be applied for this process to afford structurally diverse tetrahydroprotoberberine derivatives in excellent yields. (Figure presented.).

Acetic Acid Promoted Redox Annulations with Dual C-H Functionalization

Zhu, Zhengbo,Seidel, Daniel

supporting information, p. 2841 - 2844 (2017/06/07)

Amines such as 1,2,3,4-tetrahydroisoquinoline undergo redox-neutral annulations with 2-alkylquinoline-3-carbaldehydes as well as the corresponding 4-alkyl isomers and pyridine analogues. These processes involve dual C-H bond functionalization. Acetic acid

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