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6-Isoquinolinamine,5-bromo-(9CI) is a chemical compound belonging to the isoquinoline class, which are aromatic heterocyclic organic compounds. It is characterized by the presence of a benzene ring fused to a pyridine ring and a bromine atom in its molecular structure, making it a derivative of isoquinolinamine. Due to the lack of extensive documentation on its physical and chemical properties, reactivity, and potential health hazards, it is essential to handle and use 6-Isoquinolinamine,5-bromo-(9CI) with caution and under controlled conditions.

566943-98-4

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566943-98-4 Usage

Uses

Used in Scientific Research:
6-Isoquinolinamine,5-bromo-(9CI) is used as a research chemical for various scientific studies and experiments. Its unique structure and properties make it a valuable compound for exploring new chemical reactions and syntheses.
Used in Industrial Applications:
6-Isoquinolinamine,5-bromo-(9CI) is employed in various industrial processes, where its specific chemical properties and reactivity contribute to the development of new materials and products. The exact applications may vary depending on the industry's requirements and the compound's compatibility with other materials.
Note: Since the provided materials do not specify the exact uses of 6-Isoquinolinamine,5-bromo-(9CI) in different industries, the above uses are general and may not cover all possible applications. Further research and information are needed to provide a more detailed and industry-specific list of uses.

Check Digit Verification of cas no

The CAS Registry Mumber 566943-98-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,6,6,9,4 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 566943-98:
(8*5)+(7*6)+(6*6)+(5*9)+(4*4)+(3*3)+(2*9)+(1*8)=214
214 % 10 = 4
So 566943-98-4 is a valid CAS Registry Number.

566943-98-4SDS

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-bromoisoquinolin-6-amine

1.2 Other means of identification

Product number -
Other names RW3244

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:566943-98-4 SDS

566943-98-4Upstream product

566943-98-4Downstream Products

566943-98-4Relevant academic research and scientific papers

2,4-DIARYL - SUBSTITUTED [1,8] NAPHTHYRIDINES AS KINASE INHIBITORS FOR USE AGAINST CANCER

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Paragraph 0522; 0523, (2013/05/08)

The present invention relates to novel [1,8]naphthyridine derivatives of formula (I) and to the use of such compounds in which the inhibition, regulation and/or modulation of signal transduction by ATP consuming proteins like kinases plays a role, particu

2,4- DIARYL-SUBSTITUTED [1,8] NAPHTHYRIDINES AS KINASE INHIBITORS FOR USE AGAINST CANCER

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Page/Page column 117, (2012/01/14)

The present invention relates to novel [1,8]naphthyridine derivatives of formula (I) and to the use of such compounds in which the inhibition, regulation and/or modulation of signal transduction by ATP consuming proteins like kinases playsa role, particularly to inhibitors of TGF-beta receptor kinases, and to the use of such compounds for the treatment of kinase-induced diseases, in particular for the treatment of tumors

Identification of novel and potent isoquinoline aminooxazole-based IMPDH inhibitors

Chen, Ping,Norris, Derek,Haslow, Kristin D.,Dhar, T. G. Murali,Pitts, William J.,Watterson, Scott H.,Cheney, Daniel L.,Bassolino, Donna A.,Fleener, Catherine A.,Rouleau, Katherine A.,Hollenbaugh, Diane L.,Townsend, Robert M.,Barrish, Joel C.,Iwanowicz, Edwin J.

, p. 1345 - 1348 (2007/10/03)

Screening of our in-house compound collection led to the discovery of 5-bromo-6-amino-2-isoquinoline 1 as a weak inhibitor of IMPDH. Subsequent optimization of 1 afforded a series of novel 2-isoquinolinoaminooxazole-based inhibitors, represented by 17, with single-digit nanomolar potency against the enzyme.

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