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ChemicalBook--->CAS DataBase List--->53963-10-3

53963-10-3

53963-10-3 Structure

53963-10-3 Structure
IdentificationBack Directory
[Name]

2-(6-BROMOHEXYLOXY)TETRAHYDRO-2H-PYRAN
[CAS]

53963-10-3
[Synonyms]

AURORA KA-3062
Einecs 258-891-9
(2S)-2-(6-bromohexoxy)oxane
2-(6-BROMOHEXYLOXY)TETRAHYDROPYRAN
1-BROMO-6-TETRAHYDROPYRANYLOXYHEXANE
6-TETRAHYDROPYRARYLOXY-1-BROMOHEXANE
6-Bromohexyl 2-tetrahydropyranyl ether
2-(6-BROMOHEXYLOXY)TETRAHYDRO-2H-PYRAN
6-Bromo-1-(tetrahydropyranyloxy)hexane
2-[(6-bromohexyl)oxy]tetrahydro-2h-pyra
6-Bromo-1-hexyl 2-tetrahydropyranyl ether
2H-Pyran, 2-((6-bromohexyl)oxy)tetrahydro-
2-(6-BROMOHEXYLOXY)TETRAHYDRO-2H-PYRAN ISO 9001:2015 REACH
1-Bromo-6-tetrahydropyranyloxyhexane, 6-Tetrahydropyraryloxy-1-bromohexane
6-[(Tetrahydropyran-2-yl)oxy]-1broMohexane, 6-broMo-1-(tetrahydropyranyloxy)hexane, 2-(6-broMohexyloxy)-tetrahydropyran, 1-broMo-6-(tetrahydro-2'H-pyran-2'-yl-oxy)hexane, 6-[(tetrahydro-2H-pyran-2-yl)oxy]hexyl broMide, 6-broMohexan-1-ol tetrahydropyran-2
[EINECS(EC#)]

258-891-9
[Molecular Formula]

C11H21BrO2
[MDL Number]

MFCD00057971
[MOL File]

53963-10-3.mol
[Molecular Weight]

265.19
Chemical PropertiesBack Directory
[Melting point ]

90-91℃
[Boiling point ]

125 °C0.1 mm Hg(lit.)
[density ]

1.209 g/mL at 25 °C(lit.)
[refractive index ]

n20/D 1.478(lit.)
[Fp ]

>230 °F
[storage temp. ]

2-8°C
[solubility ]

Chloroform, Dichloromethane, Dimethyl Sulfoxide, Ethyl Acetate
[form ]

Oil
[color ]

Light Yellow
[EPA Substance Registry System]

2H-Pyran, 2-[(6-bromohexyl)oxy]tetrahydro- (53963-10-3)
Safety DataBack Directory
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

2-(6-Bromohexyloxy)tetrahydro-2H-pyran may be used as a reactant in the synthesis of diethyl 6-(tetrahydropyran-2-yloxy)hexylphosphonate and 13-(tetrahydo-2H-pyran-2-yloxy)-6-tridecyn-1-ol.
[Uses]

2-(6-Bromohexyloxy)tetrahydro-2H-pyran is an intermediate in the synthesis of (4E, 11Z)-Sphingadienine-C18-1-phosphate which is a sphingoid base of sea cucumber cerebroside that may have cytotoxicity activity against human colon cancer cells.
[General Description]

2-(6-Bromohexyloxy)tetrahydro-2H-pyran can be synthesized by reacting 6-bromohexanol and pyridinium p-toluenesulfonate in anhydrous dichloromethane.
Spectrum DetailBack Directory
[Spectrum Detail]

2-(6-BROMOHEXYLOXY)TETRAHYDRO-2H-PYRAN(53963-10-3)IR
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