669556-37-0

Basic information

• Product Name: THP-PEG8-Tos
• Synonyms: THP-PEG8-Tos
• CAS NO: 669556-37-0
• Molecular Formula: C₂₄H₄₀O₁₀S
• Molecular Weight: 520.63
• Mol File: 669556-37-0.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Solubility: Soluble in DMSO, DCM, DMF
• CAS DataBase Reference: THP-PEG8-Tos(CAS DataBase Reference)
• NIST Chemistry Reference: THP-PEG8-Tos(669556-37-0)
• EPA Substance Registry System: THP-PEG8-Tos(669556-37-0)

Safety Data

• Hazardous Substances Data: 669556-37-0(Hazardous Substances Data)

Usage

Description

THP-PEG7-Tos is a PEG linker with a THP protecting group and a tosyl moiety. The THP is an alcohol protecting group that can be removed under acidic conditions. The tosyl group is a very good leaving group for nucleophilic substitution reactions. The hydrophilic PEG linker increases the water solubility of the compound in aqueous media.

Upstream product

• 2163-11-3 2-(2-tetrahydropyran-2-yloxyethanoxy)ethanol 
• 37860-51-8 tetraethylene glycol di(p-toluenesulfonate) 
• 98-59-9 p-toluenesulfonyl chloride 
• 2615-15-8 pentaethylene glycol 
• 112-60-7 Tetraethylene glycol 
• 110-87-2 3,4-dihydro-2H-pyran 
• 42607-87-4 17-(2H-tetrahydropyran-2'-yloxy)-3,6,9,12,15-pentaoxaheptadecan-1-ol 
• 42749-28-0 toluene-4-sulfonic acid 2-[2-(2-{2-[2-(2-hydroxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethyl ester 

Downstream Products

• 250330-64-4 N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-α-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 250330-65-5 N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(4-O-(α-D-glucopyranosyl)-α-D-glucopyranosyl)-β-D-glucopyranoside 
• 250330-70-2 N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-2,3,6-tri-O-acetyl-β-D-glucopyranoside 
• 250330-71-3 N-benzyloxycarbonyl-1-amino-1-deoxyhexaethylene glycol 4-O-cellobioside 
• 250330-58-6 benzyl N-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethyl]carbamate 
• 39160-70-8 3,6,9,12,15,18-hexaoxa-1-octadecyl amine 
• 669556-53-0 2-{2-[2-(2-{2-[2-(2-{2-[2-(2-benzyloxy-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-ethoxy)-ethoxy]-ethoxy}-tetrahydro-pyran 
• 86770-69-6 17-azido-3,6,9,12,15-pentaoxaheptadecan-1-ol 

Relevant articles and documents

TUNABLE PHENYLACETYLENE HOSTS

A compound, or a salt thereof, having the formula wherein Y is n is 1 or 2; each R is independently H, alkyl, substituted alkyl, a polyether moiety, carboxyl, substituted carboxyl, carbamate, substituted carbonate, carbonyloxy, alkoxy, substituted alkoxy,

Supramolecular formation of fibrous nanostructure in donor-acceptor dyad film

A novel oligothiophene and its fullerene derivative were synthesized and their film morphologies were investigated. AFM images revealed that the oligothiophene formed well-aligned fiber-like nanostructures in the film after being thermally annealed at its liquid-crystalline temperature. In the oligothiophene-fullerene dyad film, fibers were already formed in the as-cast film. Thermal annealing further enhanced the structural order and a long, partially aligned fibrous nanostructure with a width of around 10 nm and a length of as long as 200 nm was observed. Combined with the results of X-ray analysis, these features were ascribed to supramolecular self-assembly via π-π interaction of the oligothiophene groups. Photovoltaic properties of the molecules were also investigated. The Royal Society of Chemistry.

Multigram Synthesis of Well-Defined Extended Bifunctional Polyethylene Glycol (PEG) Chains

A series of novel, well-defined, unsymmetrical poly(ethylene glycol) chains of the type X(OCH2-CH2)nY (where X = protecting group; Y = nucleofuge or a different protecting group; n = 3, 6, 9, 12, 15, 18, and 24) were prepared in high yields by applying orthogonal protecting groups. The purity of the compounds was fully verified by elemental and high-resolution mass spectrometry analyses.