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Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl- is a chemical compound belonging to the class of benzopteridines, which are derivatives of pteridine. This specific compound is characterized by the presence of a benzene ring fused to the pteridine core, with two carbonyl groups at the 2 and 4 positions and two methyl groups at the 3 and 10 positions. It has a molecular formula of C10H8N4O2 and a molecular weight of 212.19 g/mol. Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl- is known for its potential biological activities and applications in the synthesis of various pharmaceuticals and agrochemicals. Its chemical structure and properties make it an interesting target for researchers in the field of organic chemistry and drug development.

4074-59-3

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4074-59-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4074-59-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,0,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4074-59:
(6*4)+(5*0)+(4*7)+(3*4)+(2*5)+(1*9)=83
83 % 10 = 3
So 4074-59-3 is a valid CAS Registry Number.
InChI:InChI=1/C12H10N4O2/c1-15-8-6-4-3-5-7(8)13-9-10(15)14-12(18)16(2)11(9)17/h3-6H,1-2H3

4074-59-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,10-dimethylbenzo[g]pteridine-2,4-dione

1.2 Other means of identification

Product number -
Other names 3,10-Dimethylisoalloxazin (VII)

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:4074-59-3 SDS

4074-59-3Relevant academic research and scientific papers

High Oxidizing Activity of 3,10-Dimethyl-8-azaisoalloxazine (8-Azaflavin) and its Synthetic Application as a Turnover Redox Catalyst under Aerobic Conditions

Yano, Yumihiko,Ohshima, Masashi,Yatsu, Isao,Sutoh, Susumu,Vasquez, Rafael E.,et al.

, p. 753 - 758 (2007/10/02)

8-Azaflavin (1) has been synthesized, and its oxidizing activity has been examined kinetically for the oxidation of N-benzyl-1,4-dihydronicotinamide (BNAH), thiols, and nitroalkanes in aqueous solution under anaerobic conditions, by means of a comparison with 3,10-dimethylisoalloxazine (2).It was found that (1) is much more reactive than (2), 41-fold for BNAH, and 1E4-1E6-fold for thiols; (1) can be used as a turnover oxidation-reduction catalyst for disulphide and aldehyde syntheses in aqueous solution under aerobic conditions.The hydrolysis of (1) and the reducing activity of the reduced (1) have been briefly examined.

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