(1Z,5Z)-1,5-Cyclooctadiene - Names and Identifiers
Name | (1Z,5Z)-1,5-Cyclooctadiene
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Synonyms | 1,5-COD (R)-TCFP-RH 1,5-Cyclooctadiene (Z,Z)-1,5-Cyclooctadiene 1,5-Cyclooctadiene (Z,Z) (1Z,5Z)-1,5-Cyclooctadiene (1Z,5Z)-Cycloocta-1,5-diene 1,5-cyclooctadiene, (1Z,5Z)- (R)-(-)-t-ButylMethyl(di-t-butylphosphinoMethyl)phosphino(1,5-cyclooctadiene) (R)-(-)-T-BUTYLMETHYL(DI-T-BUTYLPHOSPHINOMETHYL)PHOSPHINO(1,5-CYCLOOCTADIENE)RHODIUM(I) TETRAFLUOROBORATE
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CAS | 705945-70-6
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InChI | InChI=1S/C8H12/c1-2-4-6-8-7-5-3-1/h1-2,7-8H,3-6H2/b2-1-,8-7- |
(1Z,5Z)-1,5-Cyclooctadiene - Physico-chemical Properties
Molecular Formula | C22H42P2
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Molar Mass | 368.516402 |
Density | 0.88 |
Melting Point | -69.5 |
Boling Point | 151 |
Appearance | Powder |
Color | yellow to orange |
Storage Condition | Room Temprature |
Sensitive | Air Sensitive |
(1Z,5Z)-1,5-Cyclooctadiene - Introduction
(1Z,5Z)-1,5-Cyclooctadiene ((1Z,5Z)-1,5-Cyclooctadiene) is a coordination compound with the following properties:
1. appearance and state: white solid crystal.
2. solubility: soluble in some organic solvents, such as ether and chlorinated hydrocarbons.
3. Stability: relatively stable under conventional experimental conditions, but avoid contact with water and moisture.
4. Melting point: about 150-170°C.
The use of the compound mainly includes the following aspects:
1. Catalyst: As a catalyst for asymmetric synthesis reactions, such as hydrogenation, hydride transfer, carbonylation and cycloaddition reactions.
2. organic synthesis: can be used for the preparation of enantioselective organic synthesis intermediates and functional molecules.
3. Metal organic chemistry: as a reagent in the research and synthesis of organic metal compounds.
A common method for preparing this compound is through the reaction of tetrafluoroborate with (R)-(-)-tert-butylmethyl (di-tert-butylphosphinomethyl) phosphino (1,5-cyclooctadiene) rhodium (I).
For safety information, please note the following:
1. The compound may be irritating to skin, eyes and mucous membranes. Personal protective measures, such as gloves and goggles, should be taken when contacting.
2. Avoid inhaling the dust or gas of the substance to avoid respiratory irritation.
3. Avoid contact with strong oxidants and strong acids to avoid dangerous reactions.
4. please follow the relevant laboratory safety operation procedures during use.
Last Update:2024-04-10 22:40:09