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1,3-Dioxolo[4,5-g]quinazoline is a heterocyclic organic compound characterized by a fused ring structure consisting of a quinazoline ring (a tricyclic system with one benzene ring and two nitrogen atoms) and a dioxolo ring (a five-membered ring with two oxygen atoms). 1,3-Dioxolo[4,5-g]quinazoline is of interest in medicinal chemistry due to its potential applications as a scaffold in the development of new drugs, particularly in the area of anticancer agents. The unique structure of 1,3-dioxolo[4,5-g]quinazoline allows for a variety of functional group substitutions, which can be exploited to modulate its biological activity and pharmacological properties.

269-53-4

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269-53-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 269-53-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,6 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 269-53:
(5*2)+(4*6)+(3*9)+(2*5)+(1*3)=74
74 % 10 = 4
So 269-53-4 is a valid CAS Registry Number.

269-53-4SDS

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 [1,3]dioxolo[4,5-g]quinazoline

1.2 Other means of identification

Product number -
Other names 1,3-Dioxolo[4,5-g]quinazoline

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:269-53-4 SDS

269-53-4Relevant academic research and scientific papers

Electron Deficient Heteroaromatic Ammonioamidates. Part 24. N-(Quinazolin-3-io)amidates. Part 11. The Photochemistry of N-(6,7-Methylenedioxyquinazolin-3-io)amidates in Acetone

Batra-Szalai, Gisella,Fetter, Jozsef,Lempert, Karoly,Moeller, Joergen,Parkanyi, Laszlo

, p. 2003 - 2009 (2007/10/02)

N-(Quinazolin-3-io)amidates (1) may exist, depending on the nature of the groups R, R1, and R2, and in the absence of nucleophiles, as equilibrium mixtures of the monomeric (1) and dimeric (3) forms.For the first time evidence has been found for the generation of photoproducts of the dimeric forms (3) via irradiation of the quinazolinioamidates (1a-c) in acetone in which substantial amounts of the dimers (3a-c) are present.Thus, the quinazolinioamidates (1) are the only heteroaromatic ammonioamidates which are known not only to exist in three forms, viz. the monomer, the adducts (2), and the dimers (3), but also to furnish characteristic photoproducts of all three forms.

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