CAS 3810-26-2

3-Phenyl-2-cyclopenten-1-one

Description:

3-Phenyl-2-cyclopenten-1-one, with the CAS number 3810-26-2, is an organic compound characterized by its unique bicyclic structure, which consists of a cyclopentene ring fused with a phenyl group. This compound typically exhibits a yellow to brown color and is known for its aromatic properties due to the presence of the phenyl group. It has a carbonyl functional group (ketone) that contributes to its reactivity, making it a valuable intermediate in organic synthesis. The compound is often utilized in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of dyes and pigments. Its physical properties include moderate solubility in organic solvents, and it may exhibit interesting optical properties due to its conjugated system. Additionally, 3-Phenyl-2-cyclopenten-1-one may undergo various chemical reactions, such as electrophilic addition and condensation, which are common for compounds containing both aromatic and carbonyl functionalities. Overall, its structural features and reactivity make it a compound of interest in both academic and industrial chemistry.

Formula: C₁₁H₁₀O

InChI: InChI=1/C11H10O/c12-11-7-6-10(8-11)9-4-2-1-3-5-9/h1-5,8H,6-7H2

InChI key: InChIKey=UHTNKICWCQWOBM-UHFFFAOYSA-N

SMILES: O=C1C=C(CC1)C2=CC=CC=C2

Synonyms:

• 2-Cyclopenten-1-one, 3-phenyl-
• 2-cyclopenten-1-one, 3-phenyl-
• 3-Phenyl-2-cyclopentenone
• NSC 509
• 3-Phenylcyclopent-2-en-1-one
• 3-Phenyl-2-cyclopenten-1-one
• 3-Phenyl-2-cyclopenten-1-one
• 3-Phenyl-cyclopent-2-enone

3-Phenyl-2-cyclopenten-1-one

CAS: 3810-26-2

Formula: C₁₁H₁₀O

Purity: 97%

Color and Shape: Liquid

Molecular weight: 158.1965

Ref: IN-DA00CKYE

3-Phenylcyclopent-2-enone

CAS: 3810-26-2

3-Phenylcyclopent-2-enone

Purity: 97%

Molecular weight: 158.2g/mol

Ref: 54-OR1069648

3-Phenylcyclopent-2-en-1-one

CAS: 3810-26-2

3-Phenylcyclopent-2-en-1-one is a cyclic ketone that has been synthesized by irradiation of 2,4-dihydropyran with ionizing radiation. This reaction is catalyzed by a zirconium complex and has been shown to produce the desired product in high yield. 3-Phenylcyclopent-2-en-1-one can be hydrogenated to 3-(phenyl)cyclopentanone, which can then be oxidized to 3-(phenyl)cyclopentanoic acid. The use of this compound in organic synthesis has been demonstrated through the use of iminium ion intermediates.

Formula: C₁₁H₁₀O

Purity: Min. 95%

Molecular weight: 158.2 g/mol

Ref: 3D-DAA81026