3-Octyn-1-ol, 96%
3-Octyn-1-ol, 96%
3-Octyn-1-ol, 96%
3-Octyn-1-ol, 96%
Thermo Scientific Chemicals

3-Octyn-1-ol, 96%

CAS: 14916-80-4 | C8H14O | 126.199 g/mol
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Quantity:
5 g
25 g
產品號碼 L05414.06
亦稱為 L05414-06
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化學識別
CAS14916-80-4
IUPAC Nameoct-3-yn-1-ol
Molecular FormulaC8H14O
InChI KeyLRZGRGVRZSDRTK-UHFFFAOYSA-N
SMILESCCCCC#CCCO
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規格Specification Sheet規格表
Appearance (Color)Clear colorless to pale yellow
Refractive Index1.4535-1.4600 @ 20?C
FormLiquid
Assay (GC)≥95.0%
3-Octyn-1-ol, is used for a study of the reduction of acetylenic compounds, including this alcohol, to (E)-alkenes by alkali metals in liquid ammonia. Some other applications includes as corrosion inhibitor formulation, metal complex solution, solvent stabilizer, biodegradable chemical intermediate to make pharmaceuticals, chemical compound synthesis and reagents

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Octyn-1-ol, is used for a study of the reduction of acetylenic compounds, including this alcohol, to (E)-alkenes by alkali metals in liquid ammonia. Some other applications includes as corrosion inhibitor formulation, metal complex solution, solvent stabilizer, biodegradable chemical intermediate to make pharmaceuticals, chemical compound synthesis and reagents

Solubility
It is soluble in water.

Notes
Stable under normal temperatures and pressures. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Keep away from oxidizing agents.
RUO – Research Use Only

General References:

  1. S Chandrasekhar.; C Narsihmulu.; G Chandrashekar. Pd/CaCO 3 in liquid poly (ethylene glycol)(PEG): an easy and efficient recycle system for partial reduction of alkynes to cis-olefins under a hydrogen atmosphere. Tetrahedron letters. 2004, 45,(11), 2421-2423.
  2. SE Denmark.; W Pan. Intramolecular Hydrosilylation and Silicon-Assisted Cross-Coupling: An Efficient Route to Trisubstituted Homoallylic Alcohols. Organic letters. 2001, 3,(1), 61-64.
  3. For a study of the reduction of acetylenic compounds, including this alcohol, to (E)-alkenes by alkali metals in liquid ammonia, see: Eur. J. Org. Chem., 775 (1999).