5969-70-0

Basic information

• Product Name: pentacyclo[6.6.6.0~2,7~.0~9,14~.0~15,20~]icosa-2,4,6,9,11,13,15,17,19-nonaene-3,6-diol (non-preferred name)
• Synonyms: Pentacyclo[6.6.6.0~2,7~.0~9,14~.0~15,20~]icosa-2,4,6,9,11,13,15,17,19-nonaene-3,6-diol
• CAS NO: 5969-70-0
• Molecular Formula: C₂₀H₁₄O₂
• Molecular Weight: 286.324
• Mol File: 5969-70-0.mol
• Article Data: 17

Chemical Properties

• Boiling Point: 366.9°C at 760 mmHg
• Flash Point: 167°C
• Density: 1.368g/cm³
• Vapor Pressure: 6.73E-06mmHg at 25°C
• Refractive Index: 1.745
• PKA: 10.17±0.20(Predicted)
• CAS DataBase Reference: pentacyclo[6.6.6.0~2,7~.0~9,14~.0~15,20~]icosa-2,4,6,9,11,13,15,17,19-nonaene-3,6-diol (non-preferred name)(CAS DataBase Reference)
• NIST Chemistry Reference: pentacyclo[6.6.6.0~2,7~.0~9,14~.0~15,20~]icosa-2,4,6,9,11,13,15,17,19-nonaene-3,6-diol (non-preferred name)(5969-70-0)
• EPA Substance Registry System: pentacyclo[6.6.6.0~2,7~.0~9,14~.0~15,20~]icosa-2,4,6,9,11,13,15,17,19-nonaene-3,6-diol (non-preferred name)(5969-70-0)

Safety Data

• Hazardous Substances Data: 5969-70-0(Hazardous Substances Data)

Upstream product

• 60835-52-1 9,10-dihydro-9,10-[1,2]benzenoanthracene-13,16-dione 
• 3519-82-2 9,10-dihydro-9,10-[o]benzenoanthracene-1,4-dione 
• 64-19-7 acetic acid 
• 100-63-0 phenylhydrazine 
• 1711-46-2 pentacyclo[6.6.6.0(2,7).0(9,14).0(15,20)]icosa-4,9,11,13,15,17,19-heptaene-3,6-dione 
• 92-83-1 xanthene 
• 10035-10-6 hydrogen bromide 
• 120-12-7 anthracene 
• 106-51-4 p-benzoquinone 
• 1711-46-2 pentacyclo[6.6.6.0(2,7).0(9,14).0(15,20)]icosa-4,9,11,13,15,17,19-heptaene-3,6-dione 
• 1711-46-2 C₂₀H₁₄O₂ 
• 1711-46-2 4a,9,9a,10-tetrahydro-9,10-[1',2']-benzenoanthracene-1,4-dione 

Downstream Products

• 120-12-7 anthracene 
• 3519-82-2 9,10-dihydro-9,10-[o]benzenoanthracene-1,4-dione 
• 123-31-9 hydroquinone 
• 1194230-93-7 1,4-bis(4-aminophenoxy)triptycene 
• 1313406-76-6 4,4’-[(9,10-dihydro-9,10[1‘,2’]-benzenoanthracene-1,4-diyl)bis(oxy)]bis[3-(trifluoromethyl)benzenamine] 
• 1313406-77-7 1,4-bis(4-nitro-2-trifluoromethylphenoxy)triptycene 
• 1313406-75-5 1,4-bis(4-nitrophenoxy)triptycene 
• 35132-20-8 (R,R)-1,2-diphenylethylenediamine 

Relevant articles and documents

Molecular engineering of high-performance nanofiltration membranes from intrinsically microporous poly(ether-ether-ketone)

Poly(ether-ether-ketone) has received increased attention due to its high thermal and chemical stability, and high performance in various applications. However, it suffers from a semi-crystalline morphology, low fractional free volume, and poor processability, requiring the use of harsh acidic solvents, which leads to undesired sulfonation. In this work, three intrinsically microporous poly(ether-ether-ketones) (iPEEKs), incorporating spirobisindane, Tr?ger's base, and triptycene contorted structures, were developed for organic solvent nanofiltration. Molecular dynamics simulations have assisted the molecular engineering of the polymers and the understanding of the improved membrane performance through the binding energies between solvents and polymers. Application of the design principles of polymers of intrinsic microporosity has led to a paradigm shift with a notable enhancement in both the polymer properties and the subsequently fabricated nanofiltration membranes' performance. The iPEEKs showed excellent solution processability, a high surface area of 205-250 m2 g-1, and excellent thermal stability. Mechanically flexible nanofiltration membranes were prepared from N-methyl-2-pyrrolidone dope solution at iPEEK concentrations of 19-35 wt%. The molecular weight cutoff of the membranes was fine-tuned in the range of 450-845 g mol-1 displaying 2-6 fold higher permeance (3.57-11.09 L m-2 h-1 bar-1) than previous reports. The long-term stabilities were demonstrated by a 7 day continuous cross-flow filtration. This journal is

POLYMERS FOR USE IN ELECTRONIC DEVICES

In Formula I: Qa is CRX, SiRx, GeRx, PRX, or N; Qb is CRy, SiRy, GeRy, PRy, or N; R1, R2, and R3 are the same or

NOVEL COMPOUND HAVING TRIPTYCENE SKELETON AND METHOD FOR PRODUCING THE SAME

PROBLEM TO BE SOLVED: To provide a novel compound that can be used as a polymerization component of resin. SOLUTION: The present invention provides a compound represented by formula (1) (R1 and R2 independently represent a substituent, R3 each independently represent a hydroxyl group, a group [-OR4] or a halogen atom; R4 is a hydrocarbon group; m1 each independently represent an integer of 0-4; m2 is an integer of 0-2; n is an integer of 1 or greater). SELECTED DRAWING: None COPYRIGHT: (C)2019,JPOandINPIT