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1-Ethylquinazoline-2,4(1H,3H)-dione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

2217-25-6

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2217-25-6 Usage

Class

Quinazolinedione derivative

Potential applications

Pharmaceutical properties, drug discovery and development

Identified as

Potential scaffold for new drugs

Field of interest

Medicinal chemistry

Chemical structure

Interesting target for further research and development

Biological activities

Exhibits certain activities that could be harnessed for therapeutic purposes

Check Digit Verification of cas no

The CAS Registry Mumber 2217-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,1 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2217-25:
(6*2)+(5*2)+(4*1)+(3*7)+(2*2)+(1*5)=56
56 % 10 = 6
So 2217-25-6 is a valid CAS Registry Number.

2217-25-6SDS

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 1-ethylquinazoline-2,4-dione

1.2 Other means of identification

Product number -
Other names 1-Ethyl-2,4-dioxo-1,2,3,4-tetrahydroquinazoline

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:2217-25-6 SDS

2217-25-6Relevant academic research and scientific papers

Reactions of Anthranilium Salts with Nucleophiles: Adduct Formation and Rearrangement

Vander Meer, Robert K.,Olofson, R. A.

, p. 3373 - 3377 (2007/10/02)

3-Unsubstituted anthranilium salts 1 react with alcohols in the presence of bases to yield adducts 5 which rearrange to the esters 4 when refluxed in xylene.Similar processes involving 1 and cyanide or azide also have been observed.Evidence favoring benzoazetinones 2 as rearrangement intermediates is presented.The chemistry of 1 with phosphines and phosphites is also described.For example, treatment of 1c with trimethyl phosphite yields the rearranged adduct salt 14 which cleaves to the acyl phosphonate 15 when treated with triethylamine.

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