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6-Bromoquinazoline is a chemical compound characterized by the presence of a bromine atom at the 6th position on the quinazoline ring. It is a white crystalline solid with a molecular formula of C9H7BrN2 and a molecular weight of approximately 214.07 g/mol. 6-Bromoquinazoline is known for its potential applications in medicinal chemistry and pharmaceutical research.

89892-21-7

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89892-21-7 Usage

Uses

Used in Pharmaceutical Research:
6-Bromoquinazoline is used as a reagent for structure-based design of biaryl mannoside fimH inhibitors. These inhibitors are specifically designed for the treatment of urinary infections caused by bacterial pathogens, such as Escherichia coli, which express type 1 fimbriae. 6-Bromoquinazoline plays a crucial role in the development of novel therapeutic agents targeting the fimH receptor, thereby inhibiting bacterial adhesion and colonization in the urinary tract.

Check Digit Verification of cas no

The CAS Registry Mumber 89892-21-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,8,9 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89892-21:
(7*8)+(6*9)+(5*8)+(4*9)+(3*2)+(2*2)+(1*1)=197
197 % 10 = 7
So 89892-21-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H5BrN2/c9-7-1-2-8-6(3-7)4-10-5-11-8/h1-5H

89892-21-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromoquinazoline

1.2 Other means of identification

Product number -
Other names 6-Bromchinazolin

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:89892-21-7 SDS

89892-21-7Upstream product

89892-21-7Relevant academic research and scientific papers

USE OF TRIFLUOROMETHYL SUBSTITUTED BENZAMIDES IN THE TREATMENT OF NEUROLOGICAL DISORDERS

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Page/Page column 36; 37, (2008/06/13)

The invention relates to methods of using the compounds of the invention, including trifluoromethyl substituted benzamide compounds and salts thereof, as well as pharmaceutical compositions comprising the same, in the treatment of Eph receptor-related (e.g., neurological) injuries and disorders. The invention also relates to modulating the activity of an Eph receptor in a cell, stimulating neural regeneration, and reversing neuronal degeneration, by administering a compound of the invention to a cell or subject in an effective amount.

Trifluoromethyl substituted benzamides as kinase inhibitors

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Page/Page column 20, (2008/06/13)

The invention relates to trifluoromethyl substituted benzamide compounds of the formula I, pharmaceuticals comprising these compounds, their use as or for the manufacture of pharmaceuticals, particularly as inhibitors of protein kinases, especially of ephrin receptor kinases, and/or the treatment of a condition, disorder or disease state mediated by a protein kinase activity and/or a proliferative disease, methods of treatment comprising administering the compounds, especially of therapeutic and prophylactic treatment, methods for the manufacture of the compounds and novel intermediates and partial steps for their synthesis.

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