1397692-01-1

Basic information

• Product Name: 3-amino-2-benzyl-8-methoxybenzo[f]quinoxaline
• Synonyms: 3-amino-2-benzyl-8-methoxybenzo[f]quinoxaline
• CAS NO: 1397692-01-1
• Molecular Weight: 315.374
• Mol File: 1397692-01-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 3-amino-2-benzyl-8-methoxybenzo[f]quinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-2-benzyl-8-methoxybenzo[f]quinoxaline(1397692-01-1)
• EPA Substance Registry System: 3-amino-2-benzyl-8-methoxybenzo[f]quinoxaline(1397692-01-1)

Safety Data

• Hazardous Substances Data: 1397692-01-1(Hazardous Substances Data)

Upstream product

• 55379-75-4 2-amino-3-phenylpropanenitrile 
• 1078-19-9 6-methoxy-3,4-dihydro-1(2H)-naphthalenone 
• 1397691-98-3 2-amino-3-benzyl-5-(4-methoxy-2-vinylphenyl)-6-vinylpyrazine 

Downstream Products

• 1397692-03-3 3-amino-2-benzylbenzo[f]quinoxalin-8-ol (14,v-coelenteramine) 
• 1397692-04-4 12-benzyl-8-hydroxy-2-[4-(trifluoromethyl)benzyl]-11H-benz[f]imidazo[1,2-a]quinoxalin-3-one 
• 114496-03-6 12-benzyl-8-hydroxy-2-(4-hydroxybenzyl)-11H-benz[f]imidazo[1,2-a]quinoxalin-3-one 

Relevant articles and documents

NOVEL COELENTERAZINE COMPOUNDS AND METHODS OF USE

Calcium reacting photoproteins are a class of self-illuminating proteins that emit light upon contact with calcium. Fluorescent Proteins are small proteins that change the color of light when excited. Fluorescent Proteins and Calcium Activated Photoprotei

PROCESS FOR PRODUCING v-COELENTERAZINE COMPOUNDS

A simple process for producing v-coelenterazine compounds has been desired. Described is a process for producing a v-coelenterazine compound represented by general formula (II) comprising (1) the step of reacting a compound of general formula (VIII) with a methyltriphenylphosphonium salt in the presence of a base to give a compound represented by general formula (IX), (2) the step of performing a ring-closing metathesis reaction on any one selected from the group consisting of the compound represented by general formula (IX) and a compound of general formula (X) which is the compound of general formula (IX) wherein the amino is protected with R5, and then deprotecting R4 and, if any, R5 to give a v-coelenteramine compound represented by general formula (XIV), and (3) the step of reacting the compound of general formula (XIV) with a compound represented by general formula (XV) to give the compound of general formula (II).