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27314-77-8

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27314-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27314-77-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,3,1 and 4 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 27314-77:
(7*2)+(6*7)+(5*3)+(4*1)+(3*4)+(2*7)+(1*7)=108
108 % 10 = 8
So 27314-77-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H10N4O3/c1-6-9(10(15)12-11)14(17)8-5-3-2-4-7(8)13(6)16/h2-5,11,16-17H,1H3/b12-11+

27314-77-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,4-dihydroxy-N-imino-3-methylquinoxaline-2-carboxamide

1.2 Other means of identification

Product number -
Other names Drazidox [INN]

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:27314-77-8 SDS

27314-77-8Relevant academic research and scientific papers

One-pot synthesis, molecular modeling and In Vitro antibacterial activity of novel 3-(1,3,4-Oxadiazol-2-yl) quinoxaline 1,4-dioxide and pyrazolyl analogs

Waly, Mohamed Attia,Abou-Zeid, Laila,Ramadan El-Gogary, Sameh,Shalaby, Mona Abbas

experimental part, p. 32 - 41 (2012/06/18)

The new 1,3,4-oxadiazolylquinoxaline ring system was synthesized by the condensation of the quinoxaline 1,4-dioxide acid hydrazide 6 with acetyl chloride in one-pot synthesis. In which the hydrazide was refluxed in excess of acetyl chloride, acetic anhydride or acetic acid in the presence of phosphorus oxychloride forming the 1,3,4-oxadiazolylquinoxaline ring system. Molecular modeling studies have been performed to evaluate their recognition at the hDHFR bindingpocket as potential hDHFR inhibitors. The antibacterial properties of these compounds showed reasonable activities towards gram negative bacteria, Escherichia coli. Compound 20 performed appropriate complementarity study rather well; the conserved amino acids of hDHFR enzyme imitating the MTX docking pattern. Besides, compound 20 showed highest antibacterial activity against E. coli in comparison with the well known bacteriostatic chloramphenicol; the pyrazolyl analogues also have moderate affinity toward the applied bacteria.

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