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The chemical compound "10-(2,6-Dimethyl-phenyl)-5-ethyl-4a-hydroxy-3-methyl-5,10-dihydro-4aH-benzo[g]pteridine-2,4-dione" is a complex organic molecule with a unique structure. It belongs to the class of pteridines, which are heterocyclic compounds with a pyrimido[4,5-b]pyrazine core. This specific compound features a benzo[g]pteridine scaffold, which is a type of pteridine with a benzene ring fused to the pyrimido[4,5-b]pyrazine system. The molecule is characterized by the presence of a 2,6-dimethylphenyl group at the 10-position, an ethyl group at the 5-position, a hydroxyl group at the 4a-position, and a methyl group at the 3-position. The compound also has a 5,10-dihydro structure, indicating the presence of two hydrogen atoms in the molecule that are not part of the aromatic rings, and a 4aH-benzo[g]pteridine-2,4-dione functional group, which includes a carbonyl group at both the 2 and 4 positions. 10-(2,6-Dimethyl-phenyl)-5-ethyl-4a-hydroxy-3-methyl-5,10-dihydro-4aH-benzo[g]pteridine-2,4-dione is of interest in the field of organic chemistry and may have potential applications in pharmaceuticals or as a chemical intermediate.

76030-62-1

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76030-62-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76030-62-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,0,3 and 0 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 76030-62:
(7*7)+(6*6)+(5*0)+(4*3)+(3*0)+(2*6)+(1*2)=111
111 % 10 = 1
So 76030-62-1 is a valid CAS Registry Number.

76030-62-1Downstream Products

76030-62-1Relevant academic research and scientific papers

A MODEL FOR FAD-CONTAINING MONOOXYGENASE : THE OXYDATION OF THIOANISOLE DERIVATES BY AN ISOALLOXAZINE HYDROPEROXIDE

Miller, Audrey

, p. 753 - 756 (2007/10/02)

A 4a-isoalloxazine hydroperoxide oxidizes thioanisole derivates to corresponding sulfoxides by a mechanism which involves nucleophilic attack of sulfur on electrophilic oxygen.

Products of the Decomposition of the Anion of a 4a-Hydroperoxyisoalloxazine Hindered in the 9a and 10a Positions

Bruice, Thomas C.,Miller, Audrey

, p. 693 - 694 (2007/10/02)

Products formed from the decomposition of the 4a-peroxy-anion of the flavin (1d) are only accountable through reactions involving the 4a-hydroperoxide anion; kinetic and product studies both argue against the involvement of a 4a -> 10a peroxy-anion migration.

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