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528852-07-5

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528852-07-5 Usage

Description

5-Bromo-5,6,7,8-tetrahydroquinoxaline is a heterocyclic organic compound with a molecular formula C8H9BrN2. It is a brominated derivative of tetrahydroquinoxaline, featuring a unique structure that includes a bromine atom attached to a quinoxaline ring. This chemical compound has garnered interest due to its potential applications in various fields, particularly as a building block in the synthesis of pharmaceutical drugs and agrochemicals.

Uses

Used in Pharmaceutical and Agrochemical Industries:
5-Bromo-5,6,7,8-tetrahydroquinoxaline is used as a key intermediate in the synthesis of various pharmaceutical drugs and agrochemicals. Its unique structure allows for the development of new compounds with potential therapeutic effects or as effective agents in agricultural applications.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Bromo-5,6,7,8-tetrahydroquinoxaline serves as a valuable research tool. It can be studied for its potential therapeutic effects, providing insights into the development of new drugs and treatments for various diseases and conditions.
Used in Biological Process Studies:
5-Bromo-5,6,7,8-tetrahydroquinoxaline has been the subject of scientific investigation in various fields, including the study of biological processes. Its unique properties make it a promising candidate for research into cellular mechanisms, signaling pathways, and other biological phenomena.
Overall, 5-Bromo-5,6,7,8-tetrahydroquinoxaline is a versatile chemical compound with a wide range of potential applications, making it an important substance for ongoing research and development in the pharmaceutical, agrochemical, and medicinal chemistry industries.

Check Digit Verification of cas no

The CAS Registry Mumber 528852-07-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,2,8,8,5 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 528852-07:
(8*5)+(7*2)+(6*8)+(5*8)+(4*5)+(3*2)+(2*0)+(1*7)=175
175 % 10 = 5
So 528852-07-5 is a valid CAS Registry Number.

528852-07-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-BROMO-5,6,7,8-TETRAHYDROQUINOXALINE

1.2 Other means of identification

Product number -
Other names Quinoxaline,5-bromo-5,6,7,8-tetrahydro

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:528852-07-5 SDS

528852-07-5Relevant articles and documents

Bromination of quinoxaline and derivatives: Effective synthesis of some new brominated quinoxalines

U?ar, Sefa,E?siz, Sel?uk,Da?tan, Arif

, p. 1618 - 1632 (2017/03/08)

The synthesis of brominated quinoxaline derivatives starting from several kinds of quinoxaline by different bromination strategies was studied. First the synthesis of some brominated quinoxalines was accomplished along with the development of an alternative and effective synthesis of some known compounds. A new, clean, and effective synthetic method for selective reduction of quinoxaline to 1,2,3,4-tetrahydroquinoxaline was also developed. The products obtained were characterized by means of NMR spectroscopy, elemental analyses, and mass spectrometry.

ADRENERGIC COMPOUNDS

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Page/Page column 10, (2009/04/25)

Disclosed herein is an alpha - adrenergic compound having a structure. Therapeutic methods, compositions, and medicaments for treating pain are also disclosed herein.

Enzymatic resolution of bicyclic 1-heteroarylamines using Candida antarctica lipase B

Skupinska, Krystyna A.,McEachern, Ernest J.,Baird, Ian R.,Skerlj, Renato T.,Bridger, Gary J.

, p. 3546 - 3551 (2007/10/03)

Candida antarctica lipase B has been used to kinetically resolve a structurally diverse series of bicyclic 1-heteroaryl primary amines by enantioselective acetylation. High yields of either enantiomer could be obtained with excellent enantioselectivity (90-99% ee), while the undesired enantiomer could, in some cases, be recycled by thermal racemization. The absolute stereochemistry of the products was confirmed by an X-ray crystal structure.

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