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5739-98-0

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5739-98-0 Usage

General Description

2-Hydroxy-6,7-dimethoxyquinoxaline is a chemical compound belonging to the class of organic compounds known as quinoxalines. It has a role as a metabolite and contains two methoxy groups attached to the 6 and 7 positions of its quinoxaline nucleus, along with a hydroxy group attached to the 2 position. The methoxy groups contribute to its lipophilicity, while the hydroxy group increases its water solubility. Its molecular formula is C10H10N2O3. 2-HYDROXY-6,7-DIMETHOXYQUINOXALINE has potential use in the development of pharmaceuticals and as a research tool in biochemistry and pharmacology.

Check Digit Verification of cas no

The CAS Registry Mumber 5739-98-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,3 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5739-98:
(6*5)+(5*7)+(4*3)+(3*9)+(2*9)+(1*8)=130
130 % 10 = 0
So 5739-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N2O3/c1-14-8-3-6-7(4-9(8)15-2)12-10(13)5-11-6/h3-5H,1-2H3,(H,12,13)

5739-98-0SDS

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 6,7-dimethoxy-1H-quinoxalin-2-one

1.2 Other means of identification

Product number -
Other names 6,7-dimethoxyquinoxalin-2-ol

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:5739-98-0 SDS

5739-98-0Relevant articles and documents

COMPOUNDS FOR THE TREATMENT OF MULTI-DRUG RESISTANT BACTERIAL INFECTIONS

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Page/Page column 139, (2010/11/25)

The present invention relates to compounds that demonstrate antibacterial activity, processes for their preparation, pharmaceutical compositions containing them as the active ingredient, to their use as medicaments and to their use in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans. In particular this invention relates to compounds useful for the treatment of bacterial infections in warm-blooded animals such as humans, more particularly to the use of these compounds in the manufacture of medicaments for use in the treatment of bacterial infections in warm-blooded animals such as humans.

Synthesis and SAR of novel imidazoquinoxaline-based Lck inhibitors: Improvement of cell potency

Chen, Ping,Iwanowicz, Edwin J.,Norris, Derek,Gu, Henry H.,Lin, James,Moquin, Robert V.,Das, Jagabandhu,Wityak, John,Spergel, Steven H.,De Fex, Henry,Pang, Suhong,Pitt, Sydney,Shen, Ding Ren,Schieven, Gary L.,Barrish, Joel C.

, p. 3153 - 3156 (2007/10/03)

A series of anilino(imidazoquinoxaline) analogues bearing solubilizing side chains at the 6- and 7-positions of the fused phenyl ring has been prepared and evaluated for inhibition against Lck enzyme and of T-cell proliferation. Significant improvement of the cellular activity was achieved over the initial lead, compound 2.

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