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54804-43-2

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54804-43-2 Usage

Description

Quinoxaline, 2-(bromomethyl)is a chemical compound with the molecular formula C9H7BrN2. It is a quinoxaline derivative that contains a bromomethyl group. Quinoxaline, 2-(bromomethyl)is known for its potential drug-like properties and is being explored for its pharmacological activities in the development of new therapeutic agents. It is also widely used in organic synthesis as a versatile building block for the preparation of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, it can be utilized as a reagent for the functionalization of various organic compounds.

Uses

Used in Pharmaceutical Industry:
Quinoxaline, 2-(bromomethyl)is used as a building block for the preparation of pharmaceuticals. Its unique structure allows for the development of new therapeutic agents with potential applications in various medical fields.
Used in Agrochemical Industry:
In the agrochemical industry, Quinoxaline, 2-(bromomethyl)is used as a building block for the synthesis of agrochemicals. Its versatility in organic synthesis enables the creation of new compounds with potential applications in agriculture.
Used in Organic Synthesis:
Quinoxaline, 2-(bromomethyl)is used as a versatile building block in organic synthesis. Its bromomethyl group allows for the functionalization of various organic compounds, making it a valuable reagent in the synthesis of fine chemicals.
Used in Drug Development:
Quinoxaline, 2-(bromomethyl)has demonstrated potential drug-like properties and is being explored for its pharmacological activities. It is being investigated for its potential use in the development of new therapeutic agents.
It is important to handle Quinoxaline, 2-(bromomethyl)with care as it may present health and safety hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 54804-43-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,0 and 4 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 54804-43:
(7*5)+(6*4)+(5*8)+(4*0)+(3*4)+(2*4)+(1*3)=122
122 % 10 = 2
So 54804-43-2 is a valid CAS Registry Number.

54804-43-2SDS

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-(Bromomethyl)quinoxaline

1.2 Other means of identification

Product number -
Other names 2-Brommethyl-chinoxalin

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:54804-43-2 SDS

54804-43-2Relevant articles and documents

Side chain bromination of mono and dimethyl heteroaromatic and aromatic compounds by solid phase N-bromosuccinimide reaction without radical initiator under microwave

Goswami, Shyamaprosad,Dey, Swapan,Jana, Subrata,Adak, Avijit Kumar

, p. 916 - 917 (2007/10/03)

A series of side chain mono and dibromo derivatives of mono and dimethyl heteroaromatic and aromatic compounds (1-17) were synthesized by one step solid phase N-bromosuccinimide (NBS) reaction without radical initiator by microwave irradiation. The benzylic mono and dibromo products were exclusively preferred except in the case of 6-methylpyridine amides (8 and 9) where nuclear and also side chain bromination resulted. Naphthyridine systems resulted improved yields. By this method, we also report the synthesis of 2-pivaloylaminopterin-6- carbaldehyde.

On the development of NAD(P)H-sensitive fluorescent probes

Maidwell, Nicola L.,Reza Rezai,Roeschlaub, Carl A.,Sammes, Peter G.

, p. 1541 - 1546 (2007/10/03)

In contrast to current, multi-reagent assay systems, the development of a single reagent that can be used to assay NAD(P)H is described. The reagent eliminates the fluorophore 4-methylumbelliferone from a quinoxalinium adduct upon reduction and the chemistry of this process is described. The Royal Society of Chemistry.

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