4074-59-3

Basic information

• Product Name: Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl-
• Synonyms: Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl-
• CAS NO: 4074-59-3
• Molecular Formula: C₁₂H₁₀N₄O₂
• Molecular Weight: 242.23
• Mol File: 4074-59-3.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 388.3°Cat760mmHg
• Flash Point: 188.6°C
• Appearance: /
• Density: 1.47g/cm³
• Vapor Pressure: 3.09E-06mmHg at 25°C
• Refractive Index: 1.73
• CAS DataBase Reference: Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl-(4074-59-3)
• EPA Substance Registry System: Benzo(g)pteridine-2,4(3H,10H)-dione, 3,10-dimethyl-(4074-59-3)

Safety Data

• Hazardous Substances Data: 4074-59-3(Hazardous Substances Data)

Usage

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

Upstream product

• 90828-05-0 3,10-dimethyl-5,10-dihydro-1H-benzo[g]pteridine-2,4-dione 
• 45985-24-8 TEMPOL 
• 96625-89-7 3-Methyl-6-methylamino-5-phenylamino-1H-pyrimidine-2,4-dione 
• 96625-98-8 3-Methyl-6-methylamino-5-[(E)-phenylimino]-5H-pyrimidine-2,4-dione 

Downstream Products

• 90828-05-0 3,10-dimethyl-5,10-dihydro-1H-benzo[g]pteridine-2,4-dione 
• 1892-29-1 bis(2-hydroxyethyl) disulfide 
• 71-43-2 benzene 
• 882-33-7 diphenyldisulfane 
• 2503-55-1 N-benzylnicotinamide 

Relevant articles and documents

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

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.