25163-62-6

Basic information

• Product Name: 3,6-Bis(morpholinomethyl)catechol
• Synonyms: 3,6-Bis(morpholinomethyl)-1,2-benzenediol;3,6-Bis(morpholinomethyl)catechol;3,6-bis(morpholin-4-ylmethyl)benzene-1,2-diol
• CAS NO: 25163-62-6
• Molecular Formula: C₁₆H₂₄N₂O₄
• Molecular Weight: 308.3728
• Mol File: 25163-62-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 465.5°Cat760mmHg
• Flash Point: 235.3°C
• Appearance: /
• Density: 1.278g/cm³
• Vapor Pressure: 2.74E-09mmHg at 25°C
• Refractive Index: 1.605
• CAS DataBase Reference: 3,6-Bis(morpholinomethyl)catechol(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-Bis(morpholinomethyl)catechol(25163-62-6)
• EPA Substance Registry System: 3,6-Bis(morpholinomethyl)catechol(25163-62-6)

Safety Data

• Hazardous Substances Data: 25163-62-6(Hazardous Substances Data)

Usage

InChI:InChI=1/C16H24N2O4/c19-15-13(11-17-3-7-21-8-4-17)1-2-14(16(15)20)12-18-5-9-22-10-6-18/h1-2,19-20H,3-12H2

Upstream product

• 110-91-8 morpholine 
• 50-00-0 formaldehyd 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 72744-94-6 4,5-di-morpholin-4-yl-3,6-bis-morpholin-4-ylmethyl-[1,2]benzoquinone 
• 264906-79-8 C₂₄H₄₀N₂O₄ 
• 85544-72-5 Acetic acid 2-acetoxy-3,6-dimethyl-phenyl ester 
• 1609984-67-9 (E)-3-(3,4-bis(benzyloxy)-2,5-dimethylphenyl)prop-2-en-1-ol 
• 1609984-68-0 (E)-ethyl 3-(3,4-bis(benzyloxy)-2,5-dimethylphenyl)acrylate 
• 1609984-69-1 C₄₅H₄₂O₅ 
• 97073-45-5 3,4-bis(benzyloxy)-2,5-dimethylbenzaldehyde 
• 97073-42-2 3,4-dihydroxy-2,5-dimethylbenzaldehyde 
• 93484-95-8 3,6-Bis-brommethyl-2-acetoxyphenol 
• 6452-99-9 2,3-diacetoxy-1,4-bis-bromomethyl-benzene 
• 2785-78-6 3,6-Dimethylcatechol 
• 6452-94-4 3,6-bis(acetoxymethyl)catechol diacetate 

Relevant articles and documents

Blue-Greenish Electroluminescent Poly(p-phenylenevinylene) Developed for Organic Light-Emitting Diode Applications

A novel electroluminescent poly(p-phenylenevinylene) (PPV) derivative was synthesized via the Gilch route, which emits in the blue-greenish region. The required monomer synthesis is a multistep process starting from catechol and does not involve any criti

Bis(1,3-dithiole-2-chalcogenones) and tetrathiafulvalenes in the synthesis of bridged tetrathiafulvalene-containing structures

Bis(1,3-dithiole-2-chalcogenones) in which the 1,3-dithiole fragments are linked through various bridging groups were synthesized by different methods. Some of these compounds were converted into substituted tetrathiafulvalenes with bridged 1,3-dithiole rings. The same structures were synthesized from preliminarily prepared symmetric tetrathiafulvalenes containing 2-cyanoethylsulfanyl groups in both 1,3-dithiole rings. Similar spacers were used to bridge two tetrathiafulvalene fragments. Syntheses of the involved initial compounds were described.

Efficient blue-green light emitting poly(1,4-phenylene vinylene) copolymers

2,3-Dialkoxy-substituted poly(1,4-phenylene vinylene) (PPV) homo- and co-polymers have been prepared by the Gilch dehydrohalogenation polycondensation of the corresponding bishalomethyl-substituted benzene monomers, and double layer light emitting devices