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6-AMINO-1H-QUINAZOLINE-2,4-DIONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

54243-58-2

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54243-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 54243-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,2,4 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 54243-58:
(7*5)+(6*4)+(5*2)+(4*4)+(3*3)+(2*5)+(1*8)=112
112 % 10 = 2
So 54243-58-2 is a valid CAS Registry Number.

54243-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-1H-quinazoline-2,4-dione

1.2 Other means of identification

Product number -
Other names 2,4(1H,3H)-Quinazolinedione,6-amino

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:54243-58-2 SDS

54243-58-2Relevant academic research and scientific papers

Synthesis and biological evaluation of new glutamic acid-based inhibitors of MurD ligase

Tomasic, Tihomir,Zidar, Nace,Rupnik, Veronika,Kovac, Andreja,Blanot, Didier,Gobec, Stanislav,Kikelj, Danijel,Masic, Lucija Peterlin

scheme or table, p. 153 - 157 (2009/05/07)

Mur ligases catalyze the biosynthesis of the UDP-MurNAc-pentapeptide precursor of peptidoglycan, an essential polymer of bacterial cell-wall. They constitute attractive targets for the development of novel antibacterial agents. Here we report on the synth

Indandione bis-azomethine pigments

-

, (2008/06/13)

An indandione pigment having high tinting strength and good weatherability and light fastness of the formula STR1 WHEREIN A is a phenylene or naphthylene group optionally substituted by a halogen atom, a lower alkyl group, a lower alkoxy group or a nitro group; n is 2 or 1; and B represents a direct bond or an n valont aromatic radical. The pigment mentioned above can be prepared by reacting an indandione derivative of the formula STR2 (E is an alkoxy group with 1 to 3 carbon atoms, or an amino group; and G is an oxygen atom, or STR3 in which Q is a lower alkyl group, and Q2 is a lower alkyl group or a phenyl group) with an amino compound of the formula H2 N--B--NH2 ]n-1.

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