63857-17-0

Usage

Uses

Used in Pharmaceutical Industry:
Methyl 3-oxopropanoate is used as a building block for the synthesis of various pharmaceuticals due to its versatile chemical properties and ability to be easily modified.
Used in Fragrance Industry:
Methyl 3-oxopropanoate is used as a component in the creation of fragrances due to its fruity odor and solubility in organic solvents.
Used in Organic Compounds Synthesis:
Methyl 3-oxopropanoate is used as a building block in the synthesis of various organic compounds, including other esters, ketones, and alcohols.
Used in Anti-inflammatory Applications:
Methyl 3-oxopropanoate is used as an anti-inflammatory agent due to its potential to reduce inflammation and alleviate symptoms associated with inflammatory conditions.
Used in Antioxidant Applications:
Methyl 3-oxopropanoate is used as an antioxidant to protect cells from oxidative damage and reduce the risk of various diseases associated with oxidative stress.
Used in Anticancer Applications:
Methyl 3-oxopropanoate is used as a potential anticancer agent, as it has shown promise in inhibiting the growth and progression of cancer cells. Further research is needed to fully understand its potential applications in cancer treatment.

InChI:InChI=1/C4H6O3/c1-7-4(6)2-3-5/h3H,2H2,1H3

Upstream product

• 67-56-1 methanol 
• 542-92-7 cyclopenta-1,3-diene 
• 147514-81-6 (E)-methyl 3-(1-phenylethoxy)acrylate 
• 82238-33-3 trans-9-phenylselenoxanthene 10-oxide 
• 922-67-8 propynoic acid methyl ester 

Downstream Products

• 34846-90-7 methyl 3-methoxyprop-2-enoate 
• 5751-20-2 2-Methylthiouracil 
• 137-44-0 2-pyrazolin-5-one 
• 1217351-41-1 C₃₀H₄₃BrN₂O₆ 
• 209731-38-4 4-carbomethoxy-3-(3-cyanophenyl)isoxazole 
• 25902-86-7 2-methoxy-4(3H)-pyrimidinone 
• 39687-95-1 isocyanoacetic acid methyl ester 
• 4415-07-0 3-(2,6-dichloro-phenyl)-isoxazole-4-carboxylic acid 

Relevant academic research and scientific papers

Metal complexes-catalyzed hydrolysis and alcoholysis of organic substrates and their application to kinetic resolution

Metal complexes-catalyzed hydrolysis and alcoholysis of organic substrates such as alkenyl esters, alkenyl ethers, and azlactones (oxazol-5(4H)-ones) are described. These reactions were applied for kinetic resolution of chiral compounds and high selectivities were achieved with vinyl ethers of 2-substituted cyclohexanols, 1,1′-bi-2-naphthols, 1,1′-bi-2-phenols, and 4,4-disubstituted azlactones. Oxidative carbon-carbon bond cleavage reactions, which were found in the course of the study of asymmetric hydrolysis were also described.

Difunctional and Hetercyclic Prducts from the Ozonolysis of Conjugated C5-C8 Cyclodienes

Ozonolyses of the conjugated C5-C8 cyclodienes 1a-d in methanol, followed by reduction with DMS, have been examined.Monoozonolyses gave the corresponding unsaturated dialdehydes 2e as the primary products.In subsequent reactions, the dialdehydes 2e derived from the monoozonolyses of 1a, 1b, and 1c gave in high yields the heterocyclic compounds 7, 8k, and 9k, respectively.Diozonolyses of 1a-d gave the corresponding dialdehydes 3e as the primary products.In subsequent reactions, the dialdehydes 3e derived from 1b and 1c gave the heterocyclic compounds 8l and 9l, respectively.In addition, aldehydes 2e and 3e undervent partial acetalization reactions with methanol.

STABLE SELENOXANTHENIUM YLIDES : SYNTHESIS AND NEW REDUCTIVE CYCLIZATION OF SELENOXANTHEN-10-IO(ALKOXALYL ALKOXYCARBONYL)METHANIDES AND THEIR RELATED COMPOUNDS

Stereoisomers of 9-substituted selenoxanthen-10-io(alkoxalyl alkoxycarbonyl)methanides were prepared from the corresponding selenoxides and activated acetylenes.In the reaction of 9-phenylselenoxanthene 10-oxide(1c) with methyl propiolate afforded an unexpected product, methyl 9-phenylselenoxanthen-9-ylpropiolate(5) together with ylide(2e).The selenonium ylides underwent new reductive cyclization with sodium borohydride to afford new cyclic selenonium ylides.