13865-20-8 | Methyl 2,2-dimethyl-3-oxopropanoate

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$38.00	$27.00
1g	95%	in stock	$113.00	$79.00
5g	95%	in stock	$362.00	$254.00
10g	95%	in stock	$611.00	$428.00
25g	95%	in stock	$1,193.00	$835.00

Description

• Catalog Number: AD54526
• Chemical Name: Methyl 2,2-dimethyl-3-oxopropanoate
• CAS Number: 13865-20-8
• Molecular Formula: C6H10O3
• Molecular Weight: 130.1418
• MDL Number: MFCD00082184
• SMILES: COC(=O)C(C=O)(C)C

Upstream Synthesis Route

Methyl 2,2-dimethyl-3-oxopropanoate is a versatile compound widely utilized in chemical synthesis for its valuable applications. As a key intermediate in organic chemistry, this compound serves as a crucial building block for the synthesis of various complex molecules and pharmaceuticals.Its functional groups and structural properties make it a valuable substrate for chemical reactions such as acylation, alkylation, and esterification. The presence of a carbonyl group and ester functionality in Methyl 2,2-dimethyl-3-oxopropanoate allows for diverse transformations, enabling the formation of new carbon-carbon and carbon-heteroatom bonds.In synthetic chemistry, this compound is often employed for the production of fine chemicals, agrochemicals, and pharmaceutical ingredients. By incorporating Methyl 2,2-dimethyl-3-oxopropanoate into synthetic routes, chemists can access a wide range of structurally complex molecules with diverse biological activities.Furthermore, the unique steric and electronic properties of Methyl 2,2-dimethyl-3-oxopropanoate make it a valuable reagent for controlling regioselectivity and stereoselectivity in chemical reactions. Its use in asymmetric synthesis and as a chiral building block highlights its significance in the preparation of enantiomerically pure compounds.Overall, Methyl 2,2-dimethyl-3-oxopropanoate plays a crucial role in chemical synthesis by offering a strategic starting material for the synthesis of diverse organic compounds with controlled stereochemistry and functional group patterns. Its ability to participate in a wide range of reactions makes it an essential tool for synthetic chemists seeking to access novel molecules with tailored properties.