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1049677-32-8

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1049677-32-8 Usage

General Description

The chemical 8-chloro-3-iodoimidazo[1,2-a]pyrazine is an organic compound with a molecular formula C5H3ClIN3. It is a heterocyclic compound that contains both chlorine and iodine atoms, along with an imidazole and pyrazine ring system. 8-chloro-3-iodoimidazo[1,2-a]pyrazine is used in pharmaceutical research and is being investigated for its potential medicinal properties, including its potential as an anti-cancer and anti-inflammatory agent. Its unique structure and properties make it a valuable tool for understanding the reactivity and biological activity of similar compounds. Additionally, it is used as a building block in the synthesis of various organic molecules in the field of medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1049677-32-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,9,6,7 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1049677-32:
(9*1)+(8*0)+(7*4)+(6*9)+(5*6)+(4*7)+(3*7)+(2*3)+(1*2)=178
178 % 10 = 8
So 1049677-32-8 is a valid CAS Registry Number.

1049677-32-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 8-Chloro-3-iodoimidazo[1,2-a]pyrazine

1.2 Other means of identification

Product number -
Other names -

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:1049677-32-8 SDS

1049677-32-8Relevant articles and documents

NOVEL IMIDAZO-PYRAZINE DERIVATIVES

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Page/Page column 45; 81-82, (2021/12/31)

The invention provides novel imidazo-pyrazine derivatives having the general formula (I), and pharmaceutically acceptable salts thereof, wherein X, m, n, and R1to R3 are as described herein: formula (I). Further provided are pharmace

Novel and selective TLR7 antagonists among the imidazo[1,2- a]pyrazines, Imidazo[1,5- a]quinoxalines, and Pyrazolo[1,5- a]quinoxalines Series

Bou Karroum, Nour,Moarbess, Georges,Guichou, Jean-Fran?ois,Bonnet, Pierre-Antoine,Patinote, Cindy,Bouharoun-Tayoun, Hasnaa,Chamat, Soulaima,Cuq, Pierre,Diab-Assaf, Mona,Kassab, Issam,Deleuze-Masquefa, Carine

, p. 7015 - 7031 (2019/08/20)

The Toll-like receptors (TLRs) 7 and 8 play an important role in the immune system activation, and their agonists may therefore serve as promising candidate vaccine adjuvants. However, the chronic immune activation by excessive TLR stimulation is a hallmark of several clinically important infectious and autoimmune diseases, which warrants the search for TLR antagonists. In this study, we have synthesized and characterized a variety of compounds belonging to three heterocyclic chemical series: imidazo[1,2-a]pyrazine, imidazo[1,5-a]quinoxaline, and pyrazolo[1,5-a]quinoxaline. These compounds have been tested for their TLR7 or TLR8 agonistic and antagonistic activities. Several of them are shown to be selective TLR7 antagonists without any TLR7 or TLR8 agonistic activity. The selectivity was confirmed by a comparative ligand-docking study in TLR7 antagonist pocket. Two compounds of the pyrazolo[1,5-a]quinoxaline series (10a and 10b) are potent selective TLR7 antagonists and may be considered as promising starting points for the development of new therapeutic agents.

IMIDAZOPYRAZINES FOR USE AS MPS-1 AND TKK INHIBITORS IN THE TREATMENT HYPERPROLIFERATIVE DISORDERS

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Page/Page column 40, (2012/06/30)

The present invention relates to substituted imidazopyrazine compounds of general formula (I) : in which R1, R2, R3, R4 and R5 are as defined in the claims, to methods of and intermediates for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of a hyper-proliferative and/or angiogenesis disorder, as a sole agent or in combination with other active ingredients.

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