176038-84-9

Basic information

• Product Name: Benzenemethanol, 3,5-bis(2-propynyloxy)-
• CAS NO: 176038-84-9
• Molecular Formula: C13H12O3
• Molecular Weight: 216.236
• Mol File: 176038-84-9.mol
• Article Data: 29

Chemical Properties

• CAS DataBase Reference: Benzenemethanol, 3,5-bis(2-propynyloxy)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenemethanol, 3,5-bis(2-propynyloxy)-(176038-84-9)
• EPA Substance Registry System: Benzenemethanol, 3,5-bis(2-propynyloxy)-(176038-84-9)

Safety Data

• Hazardous Substances Data: 176038-84-9(Hazardous Substances Data)

Upstream product

• 29654-55-5 5-(hydroxymethyl)benzene-1,3-diol 
• 106-96-7 propargyl bromide 
• 99-10-5 3,5-Dihydroxybenzoic acid 
• 2150-44-9 1-carbomethoxy-3,5-dihydroxybenzene 
• 624-65-7 2-propynyl chloride 
• 768387-51-5 methyl 3,5-bis(prop-2-ynyloxy)benzoate 
• 176038-83-8 2-propynyl 3,5-bis(2-propynyloxy)benzoate 

Downstream Products

• 768387-52-6 1-(chloromethyl)-3,5-bis(prop-2-yn-1-yloxy)benzene 
• 1186032-33-6 3,5-bis(prop-2-yn-1-yloxy)benzaldehyde 
• 1430325-26-0 benzene-1,3,5-tricarboxylic acid tris-(3,5-bis(2-propynyloxy))ester 
• 1123207-37-3 methyl 3,5-bis{[3,5-bis(2-propynyloxy)benzyl]oxy}benzoate 
• 1178869-01-6 C₄₁H₄₉ClN₆O₂₀ 
• 1178869-02-7 C₄₁H₄₉N₉O₂₀ 
• 1333231-61-0 S-(3,5-bis(propargyloxy)benzyl-2-amino)thiophenol 
• 1391912-05-2 C₅₁H₅₃NO₉ 
• 1242272-41-8 3,5-bis(3,5-bis(2-propynyloxy)benzyloxy)benzoic acid 
• 1123207-40-8 methyl 3,5-bis[(3,5-bis{[3,5-bis(2-propynyloxy)benzyl]oxy}benzyl)oxy]benzoate 
• 1355254-21-5 1,3,5-C₆H₃(C₆H₄-4-OCH₂C₆H₃(OCH₂CCH)2)3 
• 1361016-00-3 Br^(1-)*C₁₉H₂₆NO₂⁽¹⁺⁾ 
• 1350743-97-3 3,5-b is((3-(trimethylsilyl)prop-2-yn-1-yl)oxy)benzyl alcohol 

Relevant articles and documents

Prop-2-ynyloxybenzyloxy substituted phthalocyanine-based polymeric nanoparticles: synthesis, photophysical properties and in?vitro PDT efficacy

Two prop-2-ynyloxybenzyloxy axially/peripherally substituted zinc/silicon phthalocyanines (YSiPc and YZnPc) were synthesized. They were encapsulated into an amphiphilic block copolymeric micelle polyethylene glycol monomethyl ether-polycaprolactone (MPEG5000–PCL2000) to form polymeric nanoparticles YSiPc@MPEG5000–PCL2000 and YZnPc@MPEG5000–PCL2000. The photophysical and photochemical properties of these polymeric nanoparticles were studied by UV/Vis and fluorescence spectroscopy. The cellular uptake and reactive oxygen species (ROS) production abilities of two polymeric nanoparticles in MCF-7 breast cancer cells were evaluated by confocal laser scanning imaging. YSiPc@MPEG5000–PCL2000 exhibited a higher cellular uptake, higher ROS generation ability as well as higher photodynamic efficacy against MCF-7 cells. YSiPc@MPEG5000–PCL2000 is a promising photosensitizer for photodynamic therapy.

Clicked (AB)2C-type miktoarm terpolymers: Synthesis, thermal and self-assembly properties, and preparation of nanoporous materials

A well-defined (PEO-PS)2-PLA miktoarm terpolymer (1) was synthesized by stepwise click reactions of individually prepared poly(ethylene oxide) (PEO), polystyrene (PS, polymerized by atom transfer radical polymerization), and polylactide (PLA, p

Supramolecular redox-responsive substrate carrier activity of a ferrocenyl Janus device

Supramolecular Janus compounds have recently attracted increasing attention owing to their dynamic reversible properties, distinct topological structures, and remarkable physicochemical characteristics, e.g., amphiphilicity, heterofunctionality, and high-

Direct Enzymatic Branch-End Extension of Glycocluster-Presented Glycans: An Effective Strategy for Programming Glycan Bioactivity

The sequence of a glycan and its topology of presentation team up to determine the specificity and selectivity of recognition by saccharide receptors (lectins). Structure–activity analysis would be furthered if the glycan part of a glycocluster could be efficiently elaborated in situ while keeping all other parameters constant. By using a bacterial α2,6-sialyltransferase and a small library of bi- to tetravalent glycoclusters, we illustrate the complete conversion of scaffold-presented lactoside units into two different sialylated ligands based on N-acetyl/glycolyl-neuraminic acid incorporation. We assess the ensuing effect on their bioactivity for a plant toxin, and present an analysis of the noncovalent substrate binding contacts that the added sialic acid moiety makes to the lectin. Enzymatic diversification of a scaffold-presented glycan can thus be brought to completion in situ, offering a versatile perspective for rational glycocluster engineering.