6140-65-4 | 1-Cyclopentene-1-carbaldehyde

Packsize	Purity	Availability	Price	Discounted Price
1g	97%	in stock	$52.00	$36.00
5g	97%	in stock	$212.00	$149.00
25g	97%	in stock	$788.00	$552.00

Description

• Catalog Number: AG73933
• Chemical Name: 1-Cyclopentene-1-carbaldehyde
• CAS Number: 6140-65-4
• Molecular Formula: C6H8O
• Molecular Weight: 96.12711999999998
• MDL Number: MFCD13174425
• SMILES: O=CC1=CCCC1

Computed Properties

• Complexity: 103
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Undefined Atom Stereocenter Count: 1
• XLogP3: 1.1

Upstream Synthesis Route

The 1-Cyclopentene-1-carbaldehyde is a versatile compound used in chemical synthesis for various applications. It serves as a key building block in the creation of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure and reactivity make it an essential intermediate in the synthesis of complex organic molecules. By acting as a precursor in organic transformations, 1-Cyclopentene-1-carbaldehyde enables the formation of diverse functional groups and stereochemistries, thereby offering a wide range of possibilities for designing and accessing new molecules with desired properties.

Literature

• Synthesis of (+/-)- and (-)-vibralactone and vibralactone C.

  The Journal of organic chemistry 20081017

• Synthesis of (+/-)-vibralactone.

  Organic letters 20080403

• Structure elucidation of a pungent compound in black cardamom: Amomum tsao-ko Crevost et Lemarié (Zingiberaceae).

  Journal of agricultural and food chemistry 20071226

• The skeletal rearrangement of gold- and platinum-catalyzed cycloisomerization of cis-4,6-dien-1-yn-3-ols: pinacol rearrangement and formation of bicyclo[4.1.0]heptenone and reorganized styrene derivatives.

  Journal of the American Chemical Society 20071219

• A cyclopent-2-enecarbonyl group mimics proline at the P2 position of prolyl oligopeptidase inhibitors.

  Journal of medicinal chemistry 20041104

• 3-Formylcyclopent-3-enyl- and 3-carboxycyclopentylglycine derivatives: a new stereocontrolled approach via retro-aldol or retro-Claisen reactions.

  The Journal of organic chemistry 20030627

• Enantioselective 1,3-dipolar cycloaddition of nitrones catalyzed by optically active cationic cobalt(III) complexes.

  Organic letters 20020725