(E)-1-(Prop-1-en-1-yl)adamantane - Names and Identifiers
(E)-1-(Prop-1-en-1-yl)adamantane - Physico-chemical Properties
Molecular Formula | C13H20
|
Molar Mass | 176.3 |
Density | 1.036±0.06 g/cm3 (20 ºC 760 Torr) |
Boling Point | 230.7±7.0℃ (760 Torr) |
Flash Point | 78.6±13.0℃ |
Storage Condition | 2-8°C |
Sensitive | IRRITANT |
MDL | MFCD01321094 |
(E)-1-(Prop-1-en-1-yl)adamantane - Risk and Safety
(E)-1-(Prop-1-en-1-yl)adamantane - Introduction
Trans-1-(1-Adamantyl)Propene is an organic compound with the chemical formula C11H20. The following is a description of the properties, uses, preparation and safety information of the compound:
Nature:
-Appearance: Colorless to light yellow liquid.
-Smell: Has a special smell.
-Density: about 0.80g/cm³.
-Melting point: About -95 ° C.
-Boiling point: About 193-194 ° C.
-Solubility: Soluble in organic solvents, such as alcohols and ketones.
Use:
Trans-1-(1-Adamantyl)Propene has good high temperature stability and chemical stability, and is commonly used in the following fields:
-Industrial: Used as a chemical intermediate for the production of coatings, adhesives, plastics, etc.
-Research: Used to synthesize and study other compounds.
-Other: It can also be used as an optical ligand and a biological ligand.
Method:
Trans-1-(1-Adamantyl)Propene can be prepared by the following methods:
1. It is prepared by hydrogenation of adamantyl to alkaline conditions and co-reaction with pyridine catalyst at low temperature.
2. The intermediate is generated by the reaction of adamantyl acetone and sodium hypochlorite, and then the target product is obtained by dehydration reaction.
Safety Information:
- Trans-1-(1-Adamantyl)Propene is a flammable liquid with a pungent odor.
-Contact with skin and eyes may cause irritation and eye irritation.
-Inhalation or ingestion may cause dizziness, nausea and vomiting.
-Follow the correct working environment and safe operating procedures, including wearing chemical protective gloves, goggles and protective equipment.
-During storage and use, avoid contact with oxidants, acids, alkalis and other substances.
Last Update:2024-04-10 22:29:15