2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-, (3aS,4R,5S,6aR)- - Names and Identifiers
Name | 2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-, (3aS,4R,5S,6aR)-
|
Synonyms | 2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[... (3AS,4R,5S,6aR)-5-(Benzyloxy)-4-((benzyloxy)methyl)-hexahydro-2H-cyclopenta[b]furan-2-one (3aS,4R,5S,6aR)-Hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-2H-cyclopenta[b]furan-2-one 2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-, (3aS,4R,5S,6aR)- (3aS,4R,5S,6aR)-5-phenylmethoxy-4-(phenylmethoxymethyl)-3,3a,4,5,6,6a-hexahydrocyclopenta[b]furan-2-one 2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylMethoxy)-4-[(phenylMethoxy)Methyl]-, [3aS-(3aa,4a,5b,6aa)]-
|
CAS | 114826-79-8
|
2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-, (3aS,4R,5S,6aR)- - Physico-chemical Properties
Molecular Formula | C22H24O4
|
Molar Mass | 352.42 |
Storage Condition | 2-8°C |
Sensitive | IRRITANT |
MDL | MFCD23115468 |
2H-Cyclopenta[b]furan-2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy)methyl]-, (3aS,4R,5S,6aR)- - Introduction
(3aS,4R,5S,6aR)-2H-cyclopenta [B] furan -2-one, hexahydro-5-(phenylmethoxy)-4-[(phenylmethoxy) methyl] is an organic compound also known as cyclopentenone. The following is an introduction to its nature, use, formulation and safety information.
Nature:
-Appearance: Colorless crystalline solid
-Molecular formula: C16H20O3
-Molecular weight: 260.33g/mol
-Melting point: 72-76°C
-Boiling Point: No data available
Use:
-Cyclopentene acetone is an important organic synthesis intermediate, which is widely used in the field of drug synthesis and natural product synthesis.
-It can be further synthesized into other compounds, such as certain analgesic drugs, anticancer drugs and antibacterial drugs.
Method:
-Generally, the synthesis of cyclopentene acetone can be achieved through cyclopentenylation reaction and ketonization reaction.
The-cyclopentenylation reaction can use an alkali metal (such as sodium) or an alkali metal organic compound (such as propyl lithium) as a catalyst.
-The ketonization reaction may be carried out using an activating substrate such as an alcohol and an activating agent such as sulfuric acid.
Safety Information:
-Cyclopentene acetone should be handled and stored in accordance with general laboratory safety procedures.
-It may be irritating to the skin, eyes and respiratory system and direct contact should be avoided.
-Wear appropriate personal protective equipment such as lab gloves, goggles and protective masks when using.
Last Update:2024-04-09 02:00:41