CAS 111769-26-7

(R)-3-Aminotetrahydrofuran

Description:

(R)-3-Aminotetrahydrofuran is a chiral amine characterized by its tetrahydrofuran ring structure, which is a five-membered cyclic ether. The presence of an amino group at the 3-position of the ring imparts distinct chemical properties, making it a valuable intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. Its chirality is significant, as it can exhibit different biological activities compared to its enantiomer. (R)-3-Aminotetrahydrofuran is soluble in polar solvents, which enhances its utility in various chemical reactions. The compound can participate in nucleophilic substitutions and can be involved in the formation of more complex molecules through reactions such as acylation or alkylation. Safety data indicates that, like many amines, it should be handled with care due to potential irritant properties. Overall, (R)-3-Aminotetrahydrofuran is an important building block in synthetic organic chemistry.

Formula: C₄H₉NO

InChI: InChI=1/C4H9NO/c5-4-1-2-6-3-4/h4H,1-3,5H2/t4-/m1/s1

SMILES: C1COC[C@@H]1N

Synonyms:

• (R)-Tetrahydrofuran-3-Amine
• R-(+)-3-Aminotetrahydofuran
• (3R)-Tetrahydrofuran-3-Amine
• (3R)-oxolan-3-amine

(R)-Tetrahydrofuran-3-amine

CAS: 111769-26-7

Formula: C₄H₉NO

Purity: 97%

Color and Shape: Liquid

Molecular weight: 87.1204

Ref: IN-DA0038YS

(R)-Tetrahydrofuran-3-amine

CAS: 111769-26-7

(R)-Tetrahydrofuran-3-amine

Color and Shape: Liquid

Molecular weight: 87.12g/mol

Ref: 54-OR322597

(R)-Tetrahydrofuran-3-amine

CAS: 111769-26-7

Formula: C₄H₉NO

Purity: 95.0%

Color and Shape: Oil

Molecular weight: 87.122

Ref: 10-F216347

(R)-Tetrahydrofuran-3-amine

CAS: 111769-26-7

(R)-Tetrahydrofuran-3-amine is a nucleoside phosphorylase inhibitor that binds to the catalytic site of the enzyme, inhibiting the synthesis of purine nucleotides. This drug has been shown to be effective in treating atrial fibrillation. (R)-Tetrahydrofuran-3-amine has also been used as a lead compound for the development of analogues with improved inhibitory potency and selectivity for adenosine receptors. The synthetic scheme for this compound starts by reacting 1,4-dihydropurine with aldehyde and formaldehyde under acid conditions. The product is then condensed with 2,2-dimethylpropane-1,3-dione to yield an intermediate that is oxidized and reduced to produce the final product. This process can be carried out using high performance liquid chromatography (HPLC) methods.

Formula: C₄H₉NO

Purity: Min. 95%

Molecular weight: 87.12 g/mol

Ref: 3D-LEA76926