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7-amino-1,3-dimethyl-2,4(1H,3H)-pteridinedione, also known as acediasine, is a white to off-white crystalline powder with a molecular formula of C8H10N4O2. It is a derivative of the pteridine compound and has a molecular weight of 198.19 g/mol. Acediasine is soluble in water and dilute mineral acids and is commonly used as an intermediate in the synthesis of various pharmaceuticals, including antineoplastic and antiviral drugs. It has shown promise in pharmaceutical research for its potential therapeutic effects on certain types of cancer and viral infections.

7464-70-2

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7464-70-2 Usage

Uses

Used in Pharmaceutical Industry:
7-amino-1,3-dimethyl-2,4(1H,3H)-pteridinedione is used as an intermediate in the synthesis of various pharmaceuticals for its potential therapeutic effects on certain types of cancer and viral infections. It has been studied for its potential applications in the development of antineoplastic and antiviral drugs.
Used in Antineoplastic Drug Development:
Acediasine is used as a key intermediate in the development of antineoplastic drugs, which are used to treat cancer. It has shown potential therapeutic effects on certain types of cancer, although further research is needed to fully understand its mechanisms of action and potential applications.
Used in Antiviral Drug Development:
Acediasine is also used as an intermediate in the development of antiviral drugs, which are used to treat viral infections. It has demonstrated potential therapeutic effects against certain viral infections, and further research is required to explore its full potential in this area.

Check Digit Verification of cas no

The CAS Registry Mumber 7464-70-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 4 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7464-70:
(6*7)+(5*4)+(4*6)+(3*4)+(2*7)+(1*0)=112
112 % 10 = 2
So 7464-70-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H9N5O2/c1-12-6-5(10-3-4(9)11-6)7(14)13(2)8(12)15/h3H,1-2H3,(H2,9,11)

7464-70-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-amino-1,3-dimethylpteridine-2,4-dione

1.2 Other means of identification

Product number -
Other names 7-Amino-1,3-dimethyllumazin

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:7464-70-2 SDS

7464-70-2Relevant academic research and scientific papers

Pteridines, LXXII. - Synthesis and Properties of 6- and 7-Amino-1,3-dimethyllumazines

Steppan, Heinz,Hammer, Joachim,Baur, Ralph,Gottlieb, Raphael,Pfleiderer, Wolfgang

, p. 2135 - 2145 (2007/10/02)

The synthesis of 6- and 7-amino-, -methylamino-, and -dimethylamino-1,3-dimethyllumazines (2-4 and 12-14) is described.The nucleophilic displacement reaction proceeds easily with the 7-halo-1,3-dimethyllumazines 10, 11 whereas the amidation of 6-hydroxy-1,3-dimethyllumazine (1) with phenyl diamidophosphates is recommended for the formation of 6-amino derivatives. 6-Amino-1,3-dimethyllumazine (2) is synthesized best from 6-chloro-1,3-dimethyllumazine (7) via the 6-hydrazino derivative 5 and subsequent reduction.From pKa value determinations and UV absorption spectra of the cationic and neutral forms can be seen that protonation takes place in both series at N-5.The physical properties of the newly synthesized compounds are discussed.

pH-KONTROLLIERTE PHOTOCHEMIE VON MERCAPTOLUMAZINEN

Heckel, Armin,Pfleiderer, Wolfgang

, p. 2161 - 2164 (2007/10/02)

6-Mercapto- (1) and 7-mercapto-1,3-dimethyllumazine (2) undergo photooxidations to different reaction products depending on the present molecular form in the excited state leading to disulfides, sulfinic and sulfonic acids.

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