Cyclopropanecarboxaldehyde CAS 1489-69-6 Purity >99.0% (GC)

Cyclopropanecarboxaldehyde (CAS: 1489-69-6) reacts with Grignard or organolithium reagents to give the expected secondary alcohols. These are susceptible to ring opening in the presence of HBr, providing stereoselective access to homoallylic bromides. 
Cyclopropanecarboxaldehyde has a wide range of scientific research applications. Cyclopropanecarboxaldehyde is used as a reagent in organic synthesis and as a catalyst in the synthesis of polymers. Cyclopropanecarboxaldehyde is also used in the synthesis of pharmaceuticals, such as antibiotics and antifungal agents. In addition, Cyclopropanecarboxaldehyde is used in the synthesis of food additives, fragrances, and cosmetics.
Cyclopropanecarboxaldehyde is a member of the class of cyclopropanes, which are three-membered ring structures with one of the carbon atoms replaced by a functional group.
Cyclopropanecarboxaldehyde is a versatile intermediate in organic synthesis and is used as a starting material for the synthesis of various compounds. The compound's derivatives find applications in various fields such as agrochemicals, pharmaceuticals, and rubber chemistry. Cyclopropanecarboxaldehyde is also used in the preparation of chiral building blocks for use in asymmetric synthesis.
Cyclopropanecarboxaldehyde has a characteristic odor and is highly reactive towards nucleophiles due to the ring strain of the cyclopropane ring.