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Thermo Scientific Chemicals
(+/-)-6-Methyl-5-hepten-2-ol, 98%
CAS: 1569-60-4 | C8H16O | 128.215 g/mol
| Catalog Number | Quantity |
|---|---|
| L09181.14 also known as L09181-14 | 25 g |
Catalog number L09181.14
also known as L09181-14
Price (CNY)
-
Quantity:
25 g
Chemical Identifiers
CAS1569-60-4
IUPAC Name6-methylhept-5-en-2-ol
Molecular FormulaC8H16O
InChI KeyOHEFFKYYKJVVOX-UHFFFAOYNA-N
SMILESCC(O)CCC=C(C)C
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Specifications
Specification Sheet
Specification SheetAssay (GC)≥96.0%
Identification (FTIR)Conforms
Refractive Index1.4455-1.4505 @ 20°C
Appearance (Color)Clear colorless
FormLiquid
(±)-6-Methyl-5-hepten-2-ol is a compound used in the synthesis of aggregation pheromone of the ambrosia beetle. It is also used as pharmaceutical intermediates and insect attractant.
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
(+/-)-6-Methyl-5-hepten-2-ol is a compound used in the synthesis of aggregation pheromone of the ambrosia beetle. It is also used as pharmaceutical intermediates and insect attractant.
Solubility
Soluble in Chloroform. Not miscible with water.
Notes
Incompatible with strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
(+/-)-6-Methyl-5-hepten-2-ol is a compound used in the synthesis of aggregation pheromone of the ambrosia beetle. It is also used as pharmaceutical intermediates and insect attractant.
Solubility
Soluble in Chloroform. Not miscible with water.
Notes
Incompatible with strong oxidizing agents. Store in cool place. Keep container tightly closed in a dry and well-ventilated place.
RUO – Research Use Only
Shui-Ling Chen; Qi-Ying Hu; Teck-Peng Loh. Highly efficient chemical kinetic resolution of bishomoallylic alcohols: synthesis of (R)-sulcatol.Organic Letters.2004, 6 (19), 3365-3367.