6ALPHA, 7ALPHA-EPOXY-2-OXABICYCLO[3.3.0]OCTAN-3-ONE

6ALPHA, 7ALPHA-EPOXY-2-OXABICYCLO[3.3.0]OCTAN-3-ONE - Names and Identifiers

Name	4H-Oxireno[3,4]cyclopenta[1,2-b]furan-4-one, hexahydro-, (1aR,2aS,5aS,5bS)-rel-
Synonyms	6a,7a-epoxy-2-oxabicyclo[3.3]octan-3-one 6α,7α-Epoxy-2-oxabicyclo[3.3.0]octan-3-one 6ALPHA, 7ALPHA-EPOXY-2-OXABICYCLO[3.3.0]OCTAN-3-ONE 4H-Oxireno[3,4]cyclopenta[1,2-b]furan-4-one, hexahydro-, (1aa,2aa,5aa,5ba)- 4H-Oxireno[3,4]cyclopenta[1,2-b]furan-4-one, hexahydro-, (1aR,2aS,5aS,5bS)-rel- 4H-Oxireno[3,4]cyclopenta[1,2-b]furan-4-one,hexahydro-,(1aalpha,2aalpha,5aalpha,5balpha)-(9CI)
CAS	26115-01-5

6ALPHA, 7ALPHA-EPOXY-2-OXABICYCLO[3.3.0]OCTAN-3-ONE - Physico-chemical Properties

Molecular Formula	C7H8O3
Molar Mass	140.14
Density	1.397±0.06 g/cm3(Predicted)
Boling Point	325.7±42.0 °C(Predicted)
Storage Condition	2-8℃

6ALPHA, 7ALPHA-EPOXY-2-OXABICYCLO[3.3.0]OCTAN-3-ONE - Introduction

4h-oxirane [3,4] cyclopentyl [1,2-b]furan-one, also known as hexahydro, (1aR,2aS,5aS,5bS)-rel- (4H-Oxireno[3,4]cyclopenta[1,2-b]furan-4-one, hexahydro-, (1aR,2aS,5aS,5bS)-rel-) it is an organic compound whose chemical structure contains an oxirane ring and a cyclopentyl furan ring. Specific properties are as follows:

1. Appearance: colorless liquid or solid
2. Molecular formula: C8H12O2
3. Molecular weight: 140.18g/mol
4. Melting point:-30 ° C
5. Boiling point: 190 ° C

The main uses of this compound include but are not limited to the following:

1. Solvent: Used as a solvent in organic synthesis, it can dissolve some organic compounds, thereby promoting the reaction.
2. Intermediate: It can be used as an intermediate for the synthesis of other organic compounds, for example, for the preparation of drugs, penetrants, etc. Chemical research: Because of its unique structure and properties, it can be used in organic chemistry research, such as the exploration and understanding of reaction mechanism.

A series of organic synthesis methods can be used to prepare 4H-oxirane [3,4] cyclopentyl [1,2-b] furan-one. In general, the target compound can be obtained by synthesizing a precursor having a similar structure, and then undergoing a reaction such as epoxidation or cyclopentylfuran cyclization.

for safety information, 4H-oxirane [3,4] cyclopentane [1,2-B] The specific hazard and safety measures of the furan-ketones need to be evaluated according to the nature of the actual substance and the conditions of use. However, in general, organic compounds require certain protective measures when used and handled, such as wearing personal protective equipment, avoiding contact with skin, eyes and respiratory tract, and avoiding prolonged exposure to high temperatures. During use, please refer to the relevant safety data sheet and experimental operation guide, and ensure that the operation is under safe ventilation conditions.

Last Update：2024-04-10 22:43:14