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10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione is a complex chemical compound characterized by the presence of a pteridine ring system, a phenyl group, and a 2-methoxyethyl group. This unique molecular structure endows the compound with distinctive properties, making it a promising candidate for various applications in fields such as pharmaceuticals, dyes, and materials science.

61369-43-5

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61369-43-5 Usage

Uses

Used in Pharmaceutical Industry:
10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione is used as a pharmaceutical agent for its potential therapeutic effects. 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione's specific structure and properties may contribute to the development of new drugs for the treatment of various diseases, including cancer, inflammation, and neurological disorders.
Used in Dye Industry:
In the dye industry, 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione is used as a colorant due to its unique chromophore structure. 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione's ability to absorb and reflect light can be harnessed to create vibrant and stable dyes for various applications, such as textiles, plastics, and printing inks.
Used in Materials Science:
10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione is utilized in materials science for its potential to enhance the properties of various materials. 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione's molecular structure may contribute to the development of new materials with improved characteristics, such as increased stability, enhanced conductivity, or specific optical properties.
Used in Research and Development:
10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione is employed as a research compound for further study and exploration of its properties and potential applications. 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4(3H,10H)-dione's unique structure and characteristics make it an interesting subject for scientific investigation, which may lead to the discovery of new uses and applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 61369-43-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 61369-43:
(7*6)+(6*1)+(5*3)+(4*6)+(3*9)+(2*4)+(1*3)=125
125 % 10 = 5
So 61369-43-5 is a valid CAS Registry Number.

61369-43-5SDS

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 10-(2-methoxyethyl)-3-phenylbenzo[g]pteridine-2,4-dione

1.2 Other means of identification

Product number -
Other names -

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 -
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More Details:61369-43-5 SDS

61369-43-5Downstream Products

61369-43-5Relevant academic research and scientific papers

Nouvelle voie d'acces aux iso-alloxazines par l'intermediaire d'alkyl-1-amino-2-tetrahydro-1,5,6,7-quinoxaline-3-carbonitriles (ou carboxylate de methyle)

Lacroix, Alain,Schabat, Dominique,Clerin, Daniel,Fleury, Jean-Pierre

, p. 1065 - 1072 (2007/10/02)

A new synthetic approach to iso-alloxazines using 1-alkyl-2-amino-1,5,6,7-tetrahydroquinoxaline-3-carbonitriles (or the corresponding methylcarboxylates) is reported.These key intermediates, accessible in two steps from cyclohexanone-enamines, when treated alkyl(aryl)iso-cyanates, guanidine or alkylchloroformates yield tetrahydro-iso-alloxazine derivatives, which can be dehydrogenated.Thus 3,10-dialkyl, 10-alkyl-3-aryl, 10-alkyl-iso-alloxazines or their 2-imino-4-oxo, 4-imino-2-oxo and 2,4-bisimino derivatives were obtained.The regiospecific aspect of this approach is illustrated by the synthesis of naphto, naphto or dimethyl-7,8 benzo pteridine derivatives.Tautomeric behavior or the tetrahydro intermediates and some limitations of the method are discussed.

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