169616-08-4

Basic information

• Product Name: 6H-1,4-Dioxino[2,3-c]pyrrole-5,7-dicarboxylic acid, 2,3-dihydro-6-(phenylmethyl)-, dimethyl ester
• CAS NO: 169616-08-4
• Molecular Formula: C17H17NO6
• Molecular Weight: 331.325
• Mol File: 169616-08-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 6H-1,4-Dioxino[2,3-c]pyrrole-5,7-dicarboxylic acid, 2,3-dihydro-6-(phenylmethyl)-, dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 6H-1,4-Dioxino[2,3-c]pyrrole-5,7-dicarboxylic acid, 2,3-dihydro-6-(phenylmethyl)-, dimethyl ester(169616-08-4)
• EPA Substance Registry System: 6H-1,4-Dioxino[2,3-c]pyrrole-5,7-dicarboxylic acid, 2,3-dihydro-6-(phenylmethyl)-, dimethyl ester(169616-08-4)

Safety Data

• Hazardous Substances Data: 169616-08-4(Hazardous Substances Data)

Upstream product

• 4672-49-5 1,2-bis(methanesulfonyloxy)ethane 
• 148528-45-4 dimethyl-1-benzyl-3,4-dihydroxypyrrole-2,5-dicarboxylate 
• 106-93-4 ethylene dibromide 
• 6175-26-4 dimethyl 2,2′-(benzylazanediyl)diacetate 
• 1632-19-5 dimethyl 3,4-dihydroxy-1H-pyrrole-2,5-dicarboxylate 
• 6096-81-7 dimethyl iminodiacetate 
• 100-39-0 benzyl bromide 

Downstream Products

• 169616-13-1 3,4-ethylenedioxypyrrole-2,5-dicarboxylic acid 
• 169616-17-5 3,4-ethylenedioxypyrrole 
• 376395-17-4 N-benzyl-2-formyl-3,4-ethylenedioxypyrrole 
• 376395-16-3 6-benzyl-3,6-dihydro-2H-[1,4]dioxino[2,3-c]pyrrole 
• 376395-11-8 N-benzyl-3,4-ethylenedioxypyrrole-2,5-dicarboxylic acid 

Relevant articles and documents

Process for preparing a compound containing a heteroaromatic group with one or more ether substituents

A process for preparing a heteroaromatic compound having a heteroaromatic nucleus substituted with one or more ether groups comprising the step of: condensing at least one hydroxy-group of a compound having said heteroaromatic nucleus, said at least one hydroxy group (—OH) being substituted at α- or β-positions with respect to a heteroatom of said heteroaromatic nucleus, with an alcohol containing one or more primary or secondary alcohol groups, optionally substituted with nitro, amide, ester, halogen, cyano or (hetero)aromatic groups, using the redox couple of a triaryl- or trialkylphosphine and an azodioxo-compound at a temperature between ?40° C. and 160° C.