CAS 4720-83-6

6-Oxabicyclo[3.2.1]oct-3-en-7-one

Description:

6-Oxabicyclo[3.2.1]oct-3-en-7-one, with the CAS number 4720-83-6, is a bicyclic organic compound characterized by its unique ring structure that includes an oxygen atom in one of the rings. This compound features a bicyclo[3.2.1]octane framework, which consists of two fused cyclopentane rings and a double bond, contributing to its reactivity and stability. The presence of a ketone functional group at the 7-position enhances its electrophilic character, making it a potential candidate for various chemical reactions, including nucleophilic additions. The oxygen atom in the structure introduces polarity, influencing its solubility and interaction with other molecules. Typically, compounds like this may exhibit interesting biological activities and can serve as intermediates in synthetic organic chemistry. Its structural features may also allow for diverse applications in the development of pharmaceuticals, agrochemicals, or as building blocks in organic synthesis. Overall, 6-Oxabicyclo[3.2.1]oct-3-en-7-one is notable for its distinctive bicyclic structure and functional groups that dictate its chemical behavior.

Formula: C₇H₈O₂

InChI: InChI=1/C7H8O2/c8-7-5-2-1-3-6(4-5)9-7/h1,3,5-6H,2,4H2

SMILES: C1=CC2CC(C1)C(=O)O2

Synonyms:

• cis-6-Oxa-bicyclo3.2.1oct-3-en-7-one
• 6-OXABICYCLO[3.2.1]OCT-3-EN-7-ONE
• NSC 657815

6-OXABICYCLO[3.2.1]OCT-3-EN-7-ONE

CAS: 4720-83-6

Formula: C₇H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 124.1372

Ref: IN-DA00DELI

6-Oxabicyclo[3.2.1]oct-3-en-7-one

CAS: 4720-83-6

6-Oxabicyclo[3.2.1]oct-3-en-7-one

Purity: 98%

Ref: 54-OR1040150

6-Oxabicyclo[3.2.1]oct-3-en-7-one

CAS: 4720-83-6

Formula: C₇H₈O₂

Purity: 98%

Molecular weight: 124.139

Ref: 10-F320236

6-Oxabicyclo[3.2.1]oct-3-en-7-one

Controlled Product

CAS: 4720-83-6

Formula: C₇H₈O₂

Color and Shape: Neat

Molecular weight: 124.137

Ref: TR-E590118

6-oxabicyclo[3.2.1]oct-3-en-7-one

CAS: 4720-83-6

6-Oxabicyclo[3.2.1]oct-3-en-7-one is an initiator that belongs to the group of aminoesters. It is used for the synthesis of a variety of boronic acid esters, which are employed as cross-coupling reagents in organic synthesis reactions. The efficiency of 6-oxabicyclo[3.2.1]oct-3-en-7-one has been shown through various analyses, including sodium borohydride reduction and nucleophilic substitution reactions with secondary alkyl halides and aromatic aldehydes. 6 oxabicyclo[3.2.1]oct-3-en-7 one can be synthesized by reducing sodium borohydride with a prototropic agent or leaves in water. The reduction products are a mixture of alcohols, ketones, and hydrocarbons, which are obtained from the starting material cyclohexene

Formula: C₇H₈O₂

Purity: Min. 95%

Molecular weight: 124.14 g/mol

Ref: 3D-EAA72083