4144-55-2

Basic information

• Product Name: 4-Oxolauric acid
• Synonyms: 4-Ketolauric acid;4-Oxododecanoic acid;4-Oxolauric acid
• CAS NO: 4144-55-2
• Molecular Formula: C₁₂H₂₂O₃
• Molecular Weight: 214.3
• Mol File: 4144-55-2.mol
• Article Data: 11

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-Oxolauric acid(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Oxolauric acid(4144-55-2)
• EPA Substance Registry System: 4-Oxolauric acid(4144-55-2)

Safety Data

• Hazardous Substances Data: 4144-55-2(Hazardous Substances Data)

Upstream product

• 54050-30-5 4-oxo-dodec-2t-enoic acid 
• 33018-77-8 5-octyl-2-oxo-2,3-dihydro-furan-3,4-dicarboxylic acid diethyl ester 
• 33566-59-5 methyl 4-oxo-dodecanoate 
• 6064-56-8 3-Carboxy-3,4-dibrom-dodecansaeure 
• 17756-68-2 5-octyl-5H-furan-2-one 
• 112-80-1 cis-Octadecenoic acid 
• 127014-85-1 2,2-dimethyl-5-(2-oxodecyl)-1,3-dioxane-4,6-dione 
• 78113-07-2 Ethyl 4-ethoxycarbonyl-3-oxoundecanoate 
• 856362-66-8 1,1,1-trichloro-2-hydroxy-dodecan-4-one 
• 6404-94-0 2-nonylidenesuccinic acid 
• 137669-45-5 3-Aethoxycarbonyl-3-dodecensaeure 
• 156992-85-7 5-n-octyl-2,3-dihydrofuran 
• 55446-76-9 n-octyl-magnesium iodide 
• 39579-75-4 1-bromodecan-2-ol 

Downstream Products

• 33566-59-5 methyl 4-oxo-dodecanoate 
• 69830-92-8 5(S)-octyl-2(3H)-dihydrofuranone 
• 69830-91-7 (R)-4-dodecanolide 
• 57084-18-1 gamma-dodecalactone 

Relevant articles and documents

MODIFIED AMINE LIPIDS

The disclosure provides ionizable amine lipids and salts thereof (e.g., pharmaceutically acceptable salts thereof) useful for the delivery of biologically active agents, for example delivering biologically active agents to cells to prepare engineered cells. The ionizable amine lipids disclosed herein are useful as ionizable lipids in the formulation of lipid nanoparticle-based compositions.

Synthesis of Pseudomonas quorum-sensing autoinducer analogs and structural entities required for induction of apoptosis in macrophages

The synthesis of the analogs of N-3-oxododecanoyl-l-homoserine lactone (1) and their structure-activity relationship for the apoptotic induction in macrophages, P388D1 cells, are described. It was revealed that the position of the oxo group in the acyl si

Asymmetric hydrogenation method of a ketonic compound and derivative

The present invention relates to a process for the asymmetric hydrogenation of a ketonic compound and derivative. The invention relates to the use of optically active metal complexes as catalysts for the asymmetric hydrogenation of a ketonic compound and derivative. The process for the asymmetric hydrogenation of a ketonic compound and derivative is characterized in that the asymmetric hydrogenation of said compound is carried out in the presence of an effective amount of a metal complex comprising as ligand an optically active diphosphine corresponding to one of the following formulae: STR1