2-Allylcyclohexanone 97.0%(GC)
97.0%(GC)
Synonym: 2-prop-2-enylcyclohexan-1-one
Linear Formula:
C9H14O
Molecular Weight: 138.21g/mol
CAS Number: 94-66-6
Properties
| Assay Purity | >97%(GC) |
| Refractive index | n20/D 1.469 (lit.) |
| B pt. | 94 ℃/23 mmHg (lit.) |
| Density | 0.927 g/mL at 25 ℃ (lit.) |
Safety Information
| Hazard Statement(s) | H302 + H312 + H332-H315-H319 |
| Precautionary Statement | P501-P261-P270-P271-P264-P280-P337 + P313 -P305 + P351 + P338-P362 + P364-P332 + P313-P301 + P312 + P330-P302 + P352 + P312-P304 + P340 + P312 |
| Symbol |
|
| Signal word | Warning |
| HS Code | 2914299000 |
| Flash point | 113℃ |
| Storage Temp. | 0-10℃ |
| Storage Class | 9 |
| Packaging | Glass Bottle |
| UN Number | 3077 |
Description
Recommended products
Benzyl Phenyl Ether 98.0%(GC)
Application
2-Allylcyclohexanone may be used in the synthesis of the following bicyclo[3.3.1]non-2-en-9-one R-(-)-epilachnene an antipode of the defensive droplets from the Mexican bean beetle Epilachna varivestis.
Purpose
For R&D use onlynot for drug household or other uses.
General Description
2-Allylcyclohexanone is a -unsaturated ketone. Selective oxidation of 2-allylcyclohexanone by benzonitrile-hydrogen peroxide has been reported.[2]Asymmetric synthesis of 2-alkylcyclohexanones by alkylation of cyclohexanone enamines (III) ofL-proline ester derivatives has been described.[3]Oxidation of 2-allylcyclohexanone by 90% hydrogen peroxide catalyzed by arsonated polystyrene has been studied.
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