CAS 13865-20-8

Propanoic acid, 2,2-dimethyl-3-oxo-, methyl ester

Description:

Propanoic acid, 2,2-dimethyl-3-oxo-, methyl ester, also known by its CAS number 13865-20-8, is an organic compound characterized by its ester functional group. It features a propanoic acid backbone with a ketone and additional methyl groups, contributing to its unique structure and properties. This compound is typically a colorless to pale yellow liquid with a fruity odor, indicative of its ester nature. It is soluble in organic solvents and exhibits moderate solubility in water due to the presence of both hydrophobic and hydrophilic regions in its molecular structure. The compound is often used in organic synthesis and may serve as an intermediate in the production of various pharmaceuticals and agrochemicals. Its reactivity is influenced by the presence of the carbonyl group, making it susceptible to nucleophilic attacks. Safety data indicates that, like many organic compounds, it should be handled with care, as it may cause irritation upon contact with skin or eyes. Proper storage and handling protocols are essential to ensure safety in laboratory and industrial settings.

Formula: C₆H₁₀O₃

Methyl 2,2-dimethyl-3-oxopropanoate

CAS: 13865-20-8

Formula: C₆H₁₀O₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 130.1418

Ref: IN-DA007LPI

Methyl 2,2-dimethyl-3-oxopropanoate

CAS: 13865-20-8

Methyl 2,2-dimethyl-3-oxopropanoate

Purity: 95%

Molecular weight: 130.143g/mol

Ref: 54-OR74118

Methyl 2,2-dimethyl-3-oxopropanoate

CAS: 13865-20-8

Formula: C₆H₁₀O₃

Purity: 95%

Color and Shape: Liquid

Molecular weight: 130.143

Ref: 10-F322878

Methyl 2,2-dimethyl-3-oxopropanoate

Controlled Product

CAS: 13865-20-8

Formula: C₆H₁₀O₃

Color and Shape: Neat

Molecular weight: 130.14

Ref: TR-M335178

methyl 2,2-dimethyl-3-oxopropanoate

CAS: 13865-20-8

Methyl 2,2-dimethyl-3-oxopropanoate is an enantioselective propionate with an asymmetric synthesis. The enantiomers of methyl 2,2-dimethyl-3-oxopropanoate are separated by the use of a chiral auxiliary. The enantioselective synthesis of propionates is achieved by crotylboration, a reaction that uses boron and crotyl alcohol as substrates. Methyl 2,2-dimethyl-3-oxopropanoate is an example of a polyketide synthesized via the polyketide pathway. This compound is used in the synthesis of halipeptin, which is an antibiotic that inhibits bacterial growth by inhibiting protein synthesis and cell division.

Formula: C₆H₁₀O₃

Purity: Min. 95%

Molecular weight: 130.1 g/mol

Ref: 3D-NAA86520