113473-93-1

Basic information

• Product Name: 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene
• CAS NO: 113473-93-1
• Molecular Weight: 359.425
• Mol File: 113473-93-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene(113473-93-1)
• EPA Substance Registry System: 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene(113473-93-1)

Safety Data

• Hazardous Substances Data: 113473-93-1(Hazardous Substances Data)

Upstream product

• 95-64-7 4-amino-o-xylene 
• 50-69-1 D-ribose 
• 83916-71-6 N-ribityl-3,4-dimethylaniline 
• 62-53-3 aniline 
• 2684-02-8 benzenediazonium 
• 821787-99-9 1-(3,4-dimethyl-anilino)-D-1-deoxy-xylitol 
• 3244-40-4 1-(3,4-dimethyl-anilino)-1-deoxy-D-arabitol 
• 109215-18-1 5-(3,4-dimethyl-anilino)-5-deoxy-D-arabitol 
• 21037-26-3 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene 

Downstream Products

• 21037-26-3 1-N-D-ribitylamino-3,4-dimethyl-6-phenylazobenzene 
• 83-88-5 riboflavin 
• 146-17-8 O^5'-phosphono-riboflavin 
• 83-88-5 riboflavin 
• 752-13-6 7,8-dimethyl-10-(tetra-O-acetyl-L-arabitol-5-yl)-10H-benzo[g]pteridine-2,4-dione 
• 90467-81-5 1-N-D-2',3',4',5'-tetraacetylribitylamino-3,4-dimethyl-6-phenylazobenzene 
• 90467-81-5 1-(6-phenylazo-3.4-dimethyl-anilino)-tetra-O-acetyl-1-deoxy-D-arabitol 
• 53187-52-3 D-Lyxoflavin 
• 13123-37-0 10-L-arabitol-5-yl-7,8-dimethyl-10H-benzo[g]pteridine-2,4-dione 
• 64598-64-7 5-(2-amino-4,5-dimethyl-anilino)-5-deoxy-L-arabitol 

Relevant articles and documents

Site-Selective Synthesis of 15N- and 13C-Enriched Flavin Mononucleotide Coenzyme Isotopologues

Flavin mononucleotide (FMN) is a coenzyme for numerous proteins involved in key cellular and physiological processes. Isotopically labeled flavin is a powerful tool for studying the structure and mechanism of flavoenzyme-catalyzed reactions by a variety of techniques, including NMR, IR, Raman, and mass spectrometry. In this report, we describe the preparation of labeled FMN isotopologues enriched with 15N and 13C isotopes at various sites in the pyrazine and pyrimidine rings of the isoalloxazine core of the cofactor from readily available precursors by a five-step chemo-enzymatic synthesis.