CAS 475060-43-6

3-(iodomethyl)tetrahydrofuran

Description:

3-(Iodomethyl)tetrahydrofuran is a chemical compound characterized by its tetrahydrofuran ring structure, which is a five-membered cyclic ether. The presence of the iodomethyl group at the 3-position introduces a halogen substituent, enhancing its reactivity and making it useful in various organic synthesis applications. This compound is typically a colorless to pale yellow liquid, exhibiting moderate polarity due to the ether functionality. Its molecular structure allows for potential nucleophilic substitution reactions, making it a valuable intermediate in the synthesis of more complex molecules. Additionally, the iodomethyl group can serve as a leaving group in reactions, facilitating the formation of carbon-carbon bonds. The compound's properties, such as boiling point and solubility, are influenced by the tetrahydrofuran ring and the iodomethyl substituent. As with many halogenated compounds, it is important to handle 3-(iodomethyl)tetrahydrofuran with care due to potential toxicity and environmental concerns associated with halogenated organic compounds.

Formula: C₅H₉IO

InChI: InChI=1/C5H9IO/c6-3-5-1-2-7-4-5/h5H,1-4H2

InChI key: UJXHPFDJZCXTQR-UHFFFAOYSA-N

SMILES: C1COCC1CI

Synonyms:

• Tetrahydro-3-(iodomethyl)-furan
• 3-(Iodomethyl)Oxolane

3-(Iodomethyl)tetrahydrofuran

CAS: 475060-43-6

3-(Iodomethyl)tetrahydrofuran

Formula: C₅H₉IO

Purity: 97%

Molecular weight: 212.03

Ref: 54-OR74140

3-(Iodomethyl)tetrahydrofuran

CAS: 475060-43-6

Formula: C₅H₉IO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 212.0288

Ref: IN-DA0037U6

3-(Iodomethyl)tetrahydrofuran

CAS: 475060-43-6

3-(Iodomethyl)tetrahydrofuran

Formula: C₅H₉IO

Purity: 97%

Molecular weight: 212.03

Ref: IN-DG153445

3-(Iodomethyl)tetrahydrofuran

CAS: 475060-43-6

Formula: C₅H₉IO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 212.03

Ref: 10-F496901

Tetrahydro-3-(iodomethyl)-furan

CAS: 475060-43-6

Tetrahydro-3-(iodomethyl)-furan (THF) is a chemical compound that belongs to the group of substituted furans. It can be prepared by reacting malonic acid with ammonia and then irradiating it in a microwave. THF has been used as a precursor for the synthesis of trans-cinnamic acid, which is an organic compound that belongs to the group of cinnamic acids. Cinnamic acids are produced on a large scale in the chemical industry and are mainly used as fragrances or flavoring agents. The main application is found in synthetic flavors such as cinnamon, butter, cocoa, coffee, and licorice.

Formula: C₅H₉IO

Purity: Min. 95%

Molecular weight: 212.03 g/mol

Ref: 3D-AUA06043