| Identification | Back Directory | [Name]
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN | [CAS]
6089-04-9 | [Synonyms]
2-Propargyloxane
pent-4-ynoic acid
TIMTEC-BB SBB008982
2-Propynyl 2-pyranyl ether
Tetrahydropyran-2-yloxypropyne
2-(Propargyloxy)tetrahydropyran
2-(2-PROPYNYLOXY)TETRAHYDROPYRAN
Tetrahydropyranyl propargyl ether
Tetrahydro-2-(2-propynyloxy)pyran
3-(2'-Tetrahydropyranyloxy)propyne
3-(Tetrahydro-2-pyranyloxy)propyne
Propargyl 2-tetrahydropyranyl ether
3-(tetrahydropyran-2'-yloxy)propyne
2-(2-Propynyloxy)tetrahydro-2H-pyran
2-(prop-2-ynyloxy)tetrahydro-2H-pyran
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN
1-(2'-Tetrahydropyranyloxy)-2-propyne
2-(Prop-2-yn-1-yloxy)tetrahydro-2H-pyran
2-(2-Propynyloxy)tetrahydro-2H-pyran,98%
Tetrahydro-2-(2-propyn-1-yloxy)-2H-pyran
Tetrahydro-2-(2-propynyloxy)-2H-pyran 98%
Propargyl(tetrahydro-2H-pyran-2-yl) ether
2-Propynyl tetrahydro-2H-pyran-2-yl ether
Propargyl alcohol tetrahydropyranyl ether
2H-Pyran, tetrahydro-2-(2-propyn-1-yloxy)-
TETRAHYDRO-2-(2-PROPYNYLOXY)-2H-PYRAN, 9 8%
PROPARGYL ALCOHOL TETRAHYDRO-2H-PYRAN ETHER
(Tetrahydro-2H-pyran-2-yl)(2-propynyl) ether
2-(2-Propynyloxy)tetrahydro-2H-pyran, 98% 5GR
1-(3,4,5,6-Tetrahydro-2H-pyran-2-yloxy)-2-propyne | [EINECS(EC#)]
228-028-0 | [Molecular Formula]
C8H12O2 | [MDL Number]
MFCD00006604 | [MOL File]
6089-04-9.mol | [Molecular Weight]
140.18 |
| Chemical Properties | Back Directory | [Appearance]
Clear colorless to light yellow liquid | [Boiling point ]
63-65 °C9 mm Hg(lit.)
| [density ]
0.997 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.458(lit.)
| [Fp ]
139 °F
| [storage temp. ]
2-8°C | [form ]
Liquid | [color ]
Clear colorless to light yellow | [Specific Gravity]
0.997 | [InChI]
InChI=1S/C8H12O2/c1-2-6-9-8-5-3-4-7-10-8/h1,8H,3-7H2 | [InChIKey]
RNRIMDSCBRDPLC-UHFFFAOYSA-N | [SMILES]
C1(OCC#C)OCCCC1 | [CAS DataBase Reference]
6089-04-9 |
| Hazard Information | Back Directory | [Chemical Properties]
Clear colorless to light yellow liquid | [Uses]
Tetrahydro-2-(2-propynyloxy)-2H-pyran was used in preparation of 1,3-dienyl acetal. | [Synthesis Reference(s)]
Chemistry Letters, 6, p. 817, 1977
Organic Syntheses, Coll. Vol. 7, p. 334, 1990
Synthetic Communications, 19, p. 901, 1989 DOI: 10.1080/00397918908051010 | [General Description]
The anion formed by metalation at the acetylenic carbon reacts with a variety of electrophiles. |
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