557795-97-8

Basic information

• Product Name: DIETHYL 1-BENZYL-3,4-ETHYLENEDIOXYPYRRO&
• Synonyms: 1-benzyl-3,4-ethylenedioxypyrrole-2,5-dicarboxylate
• CAS NO: 557795-97-8
• Molecular Formula: C19H21NO6
• Molecular Weight: 359.37
• Product Categories: Conducting Polymers and Monomers;Heterocyclic Building Blocks;Organic Conductors and Photovoltaics: OFET and OPV Materials;Polypyrroles and Pyrrole MonomersBuilding Blocks;Pyrroles
• Mol File: 557795-97-8.mol

Chemical Properties

• Melting Point: 92-110 °C(lit.)
• Boiling Point: 509°C at 760 mmHg
• Flash Point: 261.6°C
• Appearance: /
• Density: 1.27g/cm³
• Vapor Pressure: 1.77E-10mmHg at 25°C
• Refractive Index: 1.574
• CAS DataBase Reference: DIETHYL 1-BENZYL-3,4-ETHYLENEDIOXYPYRRO&(CAS DataBase Reference)
• NIST Chemistry Reference: DIETHYL 1-BENZYL-3,4-ETHYLENEDIOXYPYRRO&(557795-97-8)
• EPA Substance Registry System: DIETHYL 1-BENZYL-3,4-ETHYLENEDIOXYPYRRO&(557795-97-8)

Safety Data

• Hazard Codes: Xi
• Statements: 36
• Safety Statements: 26
• Hazardous Substances Data: 557795-97-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C19H21NO6/c1-3-23-18(21)14-16-17(26-11-10-25-16)15(19(22)24-4-2)20(14)12-13-8-6-5-7-9-13/h5-9H,3-4,10-12H2,1-2H3

Upstream product

• 107-21-1 ethylene glycol 
• 376395-32-3 diethyl 1-benzyl-3,4-dihydroxy-1H-pyrrole-2,5-dicarboxylate 

Relevant articles and documents

A new and efficient synthetic route toward 3,4-alkylenedioxypyrrole (XDOP) derivatives via Mitsunobu chemistry

A new and high yielding synthetic route toward 3,4-alkylenedioxy-functionalized pyrroles has been achieved by performing tandem Mitsunobu reactions on diethyl 1-benzyl-3,4-dihydroxypyrrole-2,5-dicarboxylate using a variety of 1,2-alkanediols or 1,3-alkane

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.