Methyl (2E)-dec-2-ene-4,6-diynoate, with the CAS number 505-01-1, is an organic compound characterized by its unique structure that includes a decene backbone and two terminal alkyne groups. This compound features a methyl ester functional group, which contributes to its reactivity and solubility properties. It is typically a colorless to pale yellow liquid, exhibiting a distinct odor. The presence of multiple unsaturated bonds in its structure makes it a candidate for various chemical reactions, including polymerization and addition reactions. Methyl (2E)-dec-2-ene-4,6-diynoate is often used in organic synthesis and may serve as an intermediate in the production of more complex molecules. Its physical properties, such as boiling point and density, can vary based on environmental conditions and purity. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if inhaled or ingested. Overall, this compound is of interest in both academic research and industrial applications due to its versatile reactivity.

methyl (2E)-dec-2-ene-4,6-diynoate

505-01-1: Methyl (2E)-dec-2-ene-4,6-diynoate, with the CAS number 505-01-1, is an organic compound characterized by its unique structure that includes a decene backbone and two terminal alkyne groups. This compound features a methyl ester functional group, which contributes to its reactivity and solubility properties. It is typically a colorless to pale yellow liquid, exhibiting a distinct odor. The presence of multiple unsaturated bonds in its structure makes it a candidate for various chemical reactions, including polymerization and addition reactions. Methyl (2E)-dec-2-ene-4,6-diynoate is often used in organic synthesis and may serve as an intermediate in the production of more complex molecules. Its physical properties, such as boiling point and density, can vary based on environmental conditions and purity. As with many organic compounds, safety precautions should be taken when handling it, as it may pose health risks if inhaled or ingested. Overall, this compound is of interest in both academic research and industrial applications due to its versatile reactivity.

CAS 505-01-1

methyl (2E)-dec-2-ene-4,6-diynoate

cis-Lachnophyllum Ester

Ref: 4Z-L-176001