CAS 25662-37-7

2-Cyclohexene-1-carboxylic acid, methyl ester

Description:

2-Cyclohexene-1-carboxylic acid, methyl ester, is an organic compound characterized by its cyclohexene ring structure with a carboxylic acid functional group esterified with a methyl group. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. It is soluble in organic solvents and exhibits moderate polarity due to the presence of the ester functional group. The compound is known for its reactivity, particularly in organic synthesis, where it can participate in various chemical reactions such as esterification, hydrolysis, and polymerization. Its structure allows for potential applications in the synthesis of more complex molecules, including pharmaceuticals and agrochemicals. Safety data indicates that it should be handled with care, as it may cause irritation to the skin and eyes. As with many organic compounds, proper storage and handling protocols should be followed to ensure safety and stability.

Formula: C₈H₁₂O₂

Methyl cyclohex-2-enecarboxylate

CAS: 25662-37-7

Methyl cyclohex-2-enecarboxylate (MCHC) is a volatile compound that is found in actinomycetes and has been identified as the second major product of phenolic metabolism. MCHC is produced by the addition of an enolizable acetyl group to 2-cyclohexene-1-carboxylic acid. It can also be synthesized by the oxidation of cyclohexenyl alcohol, which is one of its main precursors. MCHC is a short-chain volatile compound that can exist as cis or trans isomers and has a boiling point of 136°C. The biosynthesis of MCHC occurs through a series of reactions that are difficult to identify because they have not yet been fully elucidated.
MCHC has been shown to cause cancer in animals, but it does not exhibit carcinogenic properties in humans because it does not bind well to DNA. The aromatic hydrocarbon content

Formula: C₈H₁₂O₂

Purity: Min. 95%

Molecular weight: 140.18 g/mol

Ref: 3D-ABA66237