79849-46-0

Basic information

• Product Name: 2H-Pyran, 2-[2-(4-bromophenyl)ethoxy]tetrahydro-
• CAS NO: 79849-46-0
• Molecular Formula: C13H17BrO2
• Molecular Weight: 285.181
• Mol File: 79849-46-0.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2H-Pyran, 2-[2-(4-bromophenyl)ethoxy]tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Pyran, 2-[2-(4-bromophenyl)ethoxy]tetrahydro-(79849-46-0)
• EPA Substance Registry System: 2H-Pyran, 2-[2-(4-bromophenyl)ethoxy]tetrahydro-(79849-46-0)

Safety Data

• Hazardous Substances Data: 79849-46-0(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 4654-39-1 4-bromophenethanol 
• 25753-12-2 (4-(2-hydroxyethyl)phenyl)(phenyl)methanone 

Downstream Products

• 105004-54-4 4-(4-Morpholinyl)benzeneethanol 
• 1353054-45-1 C₃₀H₄₄O₃ 
• 1378963-37-1 4-(9-chloro-5,6-dihydro-4H-pyrrolo[1,2-a][1,4]benzodiazepin-4-yl)benzeneethanol 
• 1018988-93-6 (RS)-di-tert-butyl(4-(2-(tetrahydro-2H-pyran-2-yloxy)ethyl)phenyl)silane 
• 70730-29-9 2-(4-(pyrrolidin-1-yl)phenyl)ethanol 
• 126202-62-8 2,6-Dimethyl-4-(3-nitro-phenyl)-1,4-dihydro-pyridine-3,5-dicarboxylic acid 3-{2-[4-(1-benzhydryl-piperidin-4-yl)-phenyl]-ethyl} ester 5-methyl ester 
• 134364-90-2 2-<4-(1-benzhydryl-4-piperidinyl)phenyl>ethyl acetate 
• 126202-72-0 2-<4-(1-benzyl-1,2,5,6-tetrahydro-4-pyridyl)phenyl>ethyl acetate 
• 134364-92-4 2-<4-(1-benzhydryl-4-piperidinyl)phenyl>ethyl alcohol 
• 126202-73-1 2-<4-(4-piperidinyl)phenyl>ethyl acetate 
• 1026872-84-3 (E)-7-{4-[2-(4-[1,3]Dioxan-2-yl-phenyl)-ethoxy]-phenyl}-7-pyridin-3-yl-hept-6-enoic acid ethyl ester 
• 1026073-46-0 (E)-7-{4-[2-(4-Formyl-phenyl)-ethoxy]-phenyl}-7-pyridin-3-yl-hept-6-enoic acid ethyl ester 
• 163164-07-6 4-(1,3-dioxan-2-yl)phenylethanol 
• 163164-47-4 4-mono(2-hydroxyethyl)benzaldehyde 

Relevant articles and documents

Original electroactive and fluorescent bichromophores based on non-conjugated tetrazine and triphenylamine derivatives: Towards more efficient fluorescent switches

The synthesis, photophysical and electrochemical properties and their interplay as well as theoretical calculations studies of newly designed fluorescent and electroactive derivatives are described. These molecules are composed of two fluorophores: one triphenylamine, electron-rich unit, and one tetrazine, electron-poor unit, connected by two different links. While in the neutral state the bichromophores are not fluorescent, due to a photoinduced electron transfer from the triphenylamine unit to the tetrazine unit, the fluorescence is restored in the oxidative state (oxidation of the triphenylamine moiety).

Benzophenone-containing fatty acids and their related photosensitive fluorescent new probes: Design, physico-chemical properties and preliminary functional investigations

Hydrophobic photoaffinity labeling is a powerful strategy to identify hydrophobic segments within molecules, in particular membrane proteins. Here we report the design and synthesis of a novel family of fluorescent and photosensitive lipid tools, which have a common amino acid scaffold functionalized by three groups: (i) a first fatty acid chain grafted with a photoactivatable benzophenone moiety (Fatty Acid BenzoPhenone, FABP), (ii) a second fatty acid chain to ensure anchoring into a half-bilayer or hydrophobic environment, and (iii) a fluorescent carboxytetramethylrhodamine headgroup (CTMR) to detect the photolabeled compound. We present data of the synthesis and characterization of three lipid tools whose benzophenone ring is situated at various distances from the central scaffold. We could therefore establish structure/properties relationships dependent upon the depth of insertion of benzophenone into the membrane. Our lipid tools were extensively characterized both physico- and bio-chemically, and we assessed their functionality in vitro using bacterioRhodopsin (bR). We thus provide the scientific community with novel and reliable tools for the identification and study of hydrophobic regions in proteins.

Silicon-derivates for PET-Imaging

This invention relates to silicon-derivated compounds suitable for labelling or already labelled with 18F, methods of preparing such a compound, compositions comprising such compounds, kits comprising such compounds or compositions and uses of such compounds, compositions or kits for diagnostic imaging, preferably positron emission tomography (PET).