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7,10-Dimethylbenzo[g]pteridine-2,4(3H,10H)-dione is a complex organic compound with the chemical formula C13H11N5O2. It is a derivative of the benzo[g]pteridine family, characterized by the presence of two methyl groups at the 7th and 10th positions, and two carbonyl groups at the 2nd and 4th positions. 7,10-Dimethylbenzo[g]pteridine-2,4(3H,10H)-dione is known for its potential role in the biosynthesis of certain biologically active molecules, such as folic acid and its derivatives, which are essential for various metabolic processes in the body. The structure of 7,10-Dimethylbenzo[g]pteridine-2,4(3H,10H)-dione features a fused ring system with a central pteridine core, which contributes to its unique chemical properties and potential applications in pharmaceutical research.

5618-84-8

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5618-84-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5618-84-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,1 and 8 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5618-84:
(6*5)+(5*6)+(4*1)+(3*8)+(2*8)+(1*4)=108
108 % 10 = 8
So 5618-84-8 is a valid CAS Registry Number.

5618-84-8SDS

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 7,10-dimethyl-10H-benzo[g]pteridine-2,4-dione

1.2 Other means of identification

Product number -
Other names 7,10-Dimethyl-10H-benzo[g]pteridin-2,4-dion

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

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More Details:5618-84-8 SDS

5618-84-8Relevant academic research and scientific papers

Linear free energy substitutent effect on flavin redox chemistry

Hasford, Justin J.,Rizzo, Carmelo J.

, p. 2251 - 2255 (2007/10/03)

A systematic study on the effect of various substituents at the 7- and/or 8-position on the redox properties of isoalloxazines (flavins) is reported. The redox properties of these flavin derivatives were studied by cyclic voltammetry in 100 mM, pH 7.4 HEPES and 200 mM, pH 10 borate buffers. The magnitude and direction of the effect was dependent on the nature and location of the substituent. The redox potentials of the substituted flavins were correlated with the Hammett σ value of the substituents.

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