151237-08-0

Basic information

• Product Name: Benzene, 1,2,3-tris(dodecyloxy)-
• CAS NO: 151237-08-0
• Molecular Formula: C42H78O3
• Molecular Weight: 631.08
• Mol File: 151237-08-0.mol
• Article Data: 16

Chemical Properties

• CAS DataBase Reference: Benzene, 1,2,3-tris(dodecyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,2,3-tris(dodecyloxy)-(151237-08-0)
• EPA Substance Registry System: Benzene, 1,2,3-tris(dodecyloxy)-(151237-08-0)

Safety Data

• Hazardous Substances Data: 151237-08-0(Hazardous Substances Data)

Upstream product

• 143-15-7 1-dodecylbromide 
• 87-66-1 2-hydroxyresorcinol 
• 112-29-8 1-bromo dodecane 

Downstream Products

• 878791-39-0 2,3,4-tris(dodecyloxy)benzenesulfonic acid 
• 878791-43-6 sodium 2,3,4-tris(dodecyloxy)benzenesulfonate 
• 878791-44-7 potassium 2,3,4-tris(dodecyloxy)benzenesulfonate 
• 1222450-39-6 C₅₀H₇₉I₂NO₃S₂ 
• 1127449-40-4 4-(3,4,5-tris(dodecyloxy)phenyl)-4H-dithieno[3,2-b:2',3'-d]pyrrole 
• 1227515-88-9 6-(2,3,4-tridodecyloxyphenyl)indolin-2,3-dione 
• 1227515-87-8 5-(2,3,4-tridodecyloxyphenyl)indolin-2,3-dione 
• 1227515-86-7 2,3,4-tridodecyloxyphenylboronic acid 
• 1227515-85-6 1-bromo-2,3,4-tridodecyloxybenzene 

Relevant articles and documents

Palladium(ii) N-heterocyclic allenylidene complexes with extended intercationic Pd?Pd interactions and MMLCT phosphorescence

Extended intercationic Pd?Pd contacts of 3.30 ? in the crystal structure and distinct MMLCT transitions absorbing at 528 nm and emitting beyond 600 nm in solutions have been revealed with cyclometalated Pd(ii) N-heterocyclic allenylidene complexes. The Pd

An electron-deficient tris(triazole)-based discotic liquid crystal that exhibits fast electron transport

In this study, a C3-symmetric star-shaped discotic mesogen has been reported based on an electron-deficient tris(triazole) central rigid core functionalized with three peripheral trialkoxyphenyl units. The mesogen exhibits an enantiotropic columnar hexagonal (Colh) phase that can sustain over a significant temperature range. When used in space-charge limited current (SCLC) devices, it showed ambipolar charge transport behavior with high electron mobility (μe) of 1.61 × 10-2 cm2 V-1 s-1 at ambient temperature. The finding is sufficiently significant to warrant their use in organic electronic devices.

Modular synthesis of polymers containing 2,5-di(thiophenyl)-N-arylpyrrole

A modular and facile route has been developed to synthesize functionalized 2,5-di(thiophen-2-yl)-1-H-arylpyrroles from readily available starting materials. These units are compatible with various polymerization conditions and are versatile building blocks for conjugated polymers. The polymers show high thermal stability and solubility in a number of solvents. Characterization of the polymers reveals a correlation between molecular packing, controllable by polymer design, and charge carrier mobility.