2-(2-Bromoethoxy)tetrahydro-2H-pyran

2-(2-Bromoethoxy)tetrahydro-2H-pyran Structure
2-(2-Bromoethoxy)tetrahydro-2H-pyran structure
Common Name 2-(2-Bromoethoxy)tetrahydro-2H-pyran
CAS Number 17739-45-6 Molecular Weight 209.081
Density 1.4±0.1 g/cm3 Boiling Point 257.8±30.0 °C at 760 mmHg
Molecular Formula C7H13BrO2 Melting Point N/A
MSDS Chinese USA Flash Point 112.5±20.1 °C
Symbol GHS07
GHS07
Signal Word Warning

Preparation of chiral ligands connected with quaternary ammonium group for recyclable catalytic asymmetric transfer hydrogenation in ionic liquid.

Chem. Pharm. Bull. 63(3) , 200-9, (2015)

Reuse of chiral ruthenium catalyst in catalytic asymmetric transfer hydrogenation (CATH) has attracted attention from economic and environmental viewpoints, and reactions using ionic liquids (ILs) as solvent are recognized as one of the most useful methods fo...

Multidentate (18)F-polypegylated styrylpyridines as imaging agents for Aβ plaques in cerebral amyloid angiopathy (CAA).

J. Med. Chem. 54(23) , 8085-98, (2011)

β-Amyloid plaques (Aβ plaques) in the brain are associated with cerebral amyloid angiopathy (CAA). Imaging agents that could target the Aβ plaques in the living human brain would be potentially valuable as biomarkers in patients with CAA. A new series of (18)...

Potent estrogen agonists based on carborane as a hydrophobic skeletal structure. A new medicinal application of boron clusters.

Chem. Biol. 8(4) , 341-55, (2001)

Carboranes (dicarba-closo-dodecaboranes) are a class of carbon-containing polyhedral boron-cluster compounds having remarkable thermal stability and exceptional hydrophobicity. Applications of the unique structural and chemical properties offered by icosahedr...

N-hydroxy-3-phenyl-2-propenamides as novel inhibitors of human histone deacetylase with in vivo antitumor activity: discovery of (2E)-N-hydroxy-3-[4-[[(2-hydroxyethyl)[2-(1H-indol-3-yl)ethyl]amino]methyl]phenyl]-2-propenamide (NVP-LAQ824).

J. Med. Chem. 46 , 4609-4624, (2003)

A series of N-hydroxy-3-phenyl-2-propenamides were prepared as novel inhibitors of human histone deacetylase (HDAC). These compounds were potent enzyme inhibitors, having IC(50)s < 400 nM in a partially purified enzyme assay. However, potency in cell growth i...

Tetrahedron Lett. 45 , 2743-2746, (2004)

Heterocycles 62 , 207-211, (2004)

Synlett , 1404, (2006)

Improved Practical Synthesis of the Sex Pheromone of Female Sweet Potato Weevil, Cylas Formicarius. Tseng J-C, et al.

Int. J. Appl. Sci. Eng. 11(3) , 293-300, (2013)