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10-hydroxybenzo[g]pteridine-2,4(3H,10H)-dione 5-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50628-74-5

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50628-74-5 Usage

Derivative of pteridine

10-hydroxybenzo[g]pteridine-2,4(3H,10H)-dione 5-oxide is derived from pteridine, which is a bicyclic heterocyclic compound.

Pteridine 5-oxide

The compound contains an oxygen atom attached to the fifth carbon of the pteridine ring, classifying it as a pteridine 5-oxide.

Widespread presence in nature

Pteridines, including this specific compound, are found in various natural sources and play essential roles in biological processes.

Role in coenzymes and pigments

Pteridines are crucial components of coenzymes and pigments, which are vital for various biological functions.

Potential applications in pharmaceuticals

Due to its unique structure and properties, 10-hydroxybenzo[g]pteridine-2,4(3H,10H)-dione 5-oxide may have possible uses in the pharmaceutical industry.

Potential applications in biochemistry

The compound could be relevant in the field of biochemistry, possibly for studying enzyme mechanisms or other biochemical processes.

Potential applications in materials science

10-hydroxybenzo[g]pteridine-2,4(3H,10H)-dione 5-oxide may also be useful in materials science, potentially for developing new materials with unique properties.

Need for further research

More research and study are required to fully understand the potential uses and effects of this specific pteridine derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 50628-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,6,2 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50628-74:
(7*5)+(6*0)+(5*6)+(4*2)+(3*8)+(2*7)+(1*4)=115
115 % 10 = 5
So 50628-74-5 is a valid CAS Registry Number.

50628-74-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 10-hydroxy-5-oxidobenzo[g]pteridin-5-ium-2,4-dione

1.2 Other means of identification

Product number -
Other names Alloxazin-5,10-dioxid

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:50628-74-5 SDS

50628-74-5Downstream Products

50628-74-5Relevant academic research and scientific papers

Synthesis and in vitro antitumor evaluation of some new pyrimido[4,5-b]quinoxaline 5,10-dioxide derivatives

Waly, Mohamed,Elgogary, Sameh,Lashien, Ahmed,Farag, Ahmad

, p. 411 - 417 (2015)

A new series of tricyclic pyrimidoquinoxaline derivatives were synthesized and evaluated as antitumor assays and compared with standard drug 5-fluorouracil. These new pyrimidoquinoxaline derivatives were synthesized by the reaction with o-aminonitrilequinoxaline derivative 3 with various reagents. One from which, the condensation of o-aminonitrile with potassium cyanate in acetic acid was stated as a new procedure for building the pyrimidine ring incorporate to quinoxaline moiety. Further condensation of aminonitrile 3 with formamide or Vilsmeier reaction followed by transamination or carbon disulphide was applied as procedures for the pyrimidine ring syntheses. Compound 15 achieved significant in vitro antitumor activity, and compounds 9 and 14 have high activities.

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