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3,6,8-Tribromo-imidazo[1,2-a]pyrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63744-24-1

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63744-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63744-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,7,4 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63744-24:
(7*6)+(6*3)+(5*7)+(4*4)+(3*4)+(2*2)+(1*4)=131
131 % 10 = 1
So 63744-24-1 is a valid CAS Registry Number.

63744-24-1SDS

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 3,6,8-Tribromoimidazo[1,2-a]pyrazine

1.2 Other means of identification

Product number -
Other names 3,6,8-Tribromo-imidazo[1,2-a]pyrazine

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:63744-24-1 SDS

63744-24-1Downstream Products

63744-24-1Relevant academic research and scientific papers

Synthesis, in vitro anticancer activity and SAR studies of arylated imidazo[1,2-a]pyrazine-coumarin hybrids

Goel, Richa,Luxami, Vijay,Paul, Kamaldeep

, p. 37887 - 37895 (2015/05/20)

A new series of imidazo[1,2-a]pyrazine-coumarin hybrids have been synthesized by the combination of two biologically active moieties, imidazo[1,2-a]pyrazine and coumarin, followed by the Suzuki-Miyaura cross coupling reaction for monoarylation at the C6 p

Structure-based design of imidazo[1,2-a]pyrazine derivatives as selective inhibitors of Aurora-A kinase in cells

Bouloc, Nathalie,Large, Jonathan M.,Kosmopoulou, Magda,Sun, Chongbo,Faisal, Amir,Matteucci, Mizio,Reynisson, Jóhannes,Brown, Nathan,Atrash, Butrus,Blagg, Julian,McDonald, Edward,Linardopoulos, Spiros,Bayliss, Richard,Bavetsias, Vassilios

scheme or table, p. 5988 - 5993 (2010/11/02)

Co-crystallisation of the imidazo[1,2-a]pyrazine derivative 15 (3-chloro-N-(4-morpholinophenyl)-6-(pyridin-3-yl)imidazo[1,2-a]pyrazin-8-amine) with Aurora-A provided an insight into the interactions of this class of compound with Aurora kinases. This led to the design and synthesis of potent Aurora-A inhibitors demonstrating up to 70-fold selectivity in cell-based Aurora kinase pharmacodynamic biomarker assays.

IMIDAZOPYRAZINE COMPOUNDS

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Page/Page column 75, (2009/04/25)

Novel imidazopyrazine compounds are disclosed that have a formula represented by the following: Formula (I). The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a viral infection, in particular a HCV, HRV, Sb and/or CVB in a patient in need thereof.

Novel imidazopyrazines as cyclin dependent kinase inhibitors

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Page/Page column 46, (2008/06/13)

In its many embodiments, the present invention provides a novel class of imidazo[1,2-a]pyrazine compounds as inhibitors of cyclin dependent kinases, methods of preparing such compounds, pharmaceutical compositions containing one or more such compounds, me

8-alkylaminoimidazo(1,2-a)pyrazines and derivatives, their preparation and their application in therapy

-

, (2008/06/13)

STR1 Novel 8-alkylamino-imidazo(1,2-a)pyrazines of formula (I) show advantages pharmacological activities. They can be used for medical products in human and veterinary therapy in the field of applications of antispasmodics, uterine relaxants, bronchodila

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