53558-93-3

Usage

Uses

1. Used in Pharmaceutical Industry:
(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID is used as an intermediate for the synthesis of 2'',3''-dideoxy-4''-selenonucleosides, which are potential antiviral agents. These compounds have the potential to be developed into new treatments for viral infections, offering a valuable contribution to the field of medicine.
2. Used in Analytical Chemistry:
(R)-(-)-5-OXOTETRAHYDROFURAN-2-CARBOXYLIC ACID is used as an HPLC (High-Performance Liquid Chromatography) derivatization reagent for UV/Vis detection. This application allows for the sensitive and selective detection of various compounds in complex samples, making it a valuable tool in the field of analytical chemistry.

InChI:InChI=1/C5H6O4/c6-4-2-1-3(9-4)5(7)8/h3H,1-2H2,(H,7,8)/p-1/t3-/m1/s1

Upstream product

• 27025-41-8 Oxidized glutathione 
• 7209-05-4 Diethyl α-chloroglutarate 
• 7664-41-7 ammonia 
• 56-86-0 L-glutamic acid 
• 328-50-7 α-ketoglutaric acid 

Downstream Products

• 7209-00-9 diethyl 2-bromoglutarate 
• 617-65-2 Glutamic acid 
• 111075-15-1 (R,S)-4-bromophenyl 5-oxotetrahydrofuran-2-carboxylate 
• 65758-34-1 1-Acetyl-1,5-dihydro-2H-pyrrolinon 
• 497-23-4 2-buten-4-olide 
• 111075-16-2 (R,S)-N-(4-bromophenyl) 5-oxotetrahydrofuran-2-carboxamide 
• 20825-71-2 2(3H)-furanone 
• 63836-94-2 Blc-His-Pro-NH2 
• 82977-45-5 tetrahydro-5-oxofuran-2-carboxylic acid chloride 
• 110-94-1 1,5-pentanedioic acid 
• 2889-31-8 2-hydroxyglutaric acid 
• 51268-87-2 (4S)-3-(2,2-dimethyl-1,3-dioxolan-4-yl)propan-1-ol 
• 171335-60-7 (2S)-5-O-benzylpentane-1,2,5-triol 
• 158010-31-2 (2S)-1,2-O-isopropylidene-5-O-benzylpentane-1,2,5-triol 

Relevant academic research and scientific papers

Metal-catalyzed reductive deamination of glutamic acid to bio-based dimethyl glutarate and methylamines

Glutamic acid is a promising renewable platform molecule which is abundantly available in biomass waste streams; it is also efficiently manufactured by fermentation. Here we report the reductive deamination of glutamic acid to bio-based dimethyl glutarate and methylamines. In order to recycle nitrogen in an industrially relevant co-product, glutamic acid was modified to N,N-dimethylglutamic acid by a mild reductive alkylation with Pd/C. Subsequently, selective C-N hydrogenolysis in methanol resulted in dimethyl glutarate and trimethylamine. A wide screening of transition metals (Pt, Pd, Rh and Ru) immobilized on various supports showed that the highest yields of dimethyl glutarate were obtained with Pt/TiO2. An FTIR study and kinetic experiments on metal-loaded and unloaded supports demonstrate that the interplay between the metal and the moderate acidity of the support results in the excellent C-N hydrogenolysis activity and selectivity. Finally, reaction parameter optimization resulted in 81% yield of dimethyl glutarate with 1 wt% Pt/TiO2 at 225 °C, 30 bar H2 after 8 h.

Investigations into the phenolic constituents of Dog's mercury (Mercurialis perennis L.) by LC-MS/MS and GC-MS analyses

Introduction Dog's mercury (Mercurialis perennis L.) is a traditional European medicinal plant considered as a rich source of bioactive natural products. Yet phytochemical data of the plant are scant. Objective This study aimed to identify the hydrophilic phenolic constituents from M. perennis by aqueous and hydroalcoholic extraction. Methodology Extracts of herbal parts were investigated in-depth by HPLC(DAD)-MS/MS and GC/MS analyses. In addition, a novel compound was isolated and fully characterised by 1- and 2D-NMR experiments. Results Several conjugates of caffeic, p-coumaric and ferulic acids together with glucaric or 2-hydroxyglutaric acids (depsides) were detected in the aqueous extracts from aerial plant parts by use of LC-MS/MS techniques as well UV-spectral data. By implementation of preparative chromatography on polyamide pretreated with formic acid followed by vacuum liquid chromatography on reversed-phase C18-silica, one of the predominant depsides was isolated as a pure compound. The NMR spectra (1H and 13C NMR) together with 2D-hetereonuclear multiple bond correlation NMR experiments (gHMBC and gHSQC) and chiral GC investigation, allowed identification of this compound as (-)-(E)-caffeoyl-2-(R)-oxoglutarate. This structure was additionally supported by GC/MS data after silylation and methylation reactions. The hydroalcoholic extract from aerial parts was separated by solvent partition between ethyl acetate and n-butanol. The latter fraction (n-butanol) yielded a mixture of mono- and oligo-glycosides of kaempferol and quercetin, all of them being assigned by LC-MS/MS. Conclusions The present investigation constitutes the first comprehensive report on the hydrophilic constituents of the rarely studied plant Mercurialis and thus completes the phytochemical knowledge on M. perennis.

Reactivite du nitrite de sodium. V. Action sur les amino-acides, peptides et proteines

The action of sodium nitrite on various amino-acids was re-examined in conditions approximating to a biological medium. 13C-NMR provides evidence of the existence of intramolecular ring closures and the formation of 5-membered rings with ornithine, citrulline and arginine.The reaction of cystine shows the opening of the sulphur bridges, whereas cysteine leads to the formation of carboxy-thiiran and 3-sulpho-lactic acid.The hydrolysis of the amide bonds of asparagine and glutamine is complete whereas the peptides studied - carnosine and aspartam - do not undergo hydrolysis of the peptide linkage.However, the first deamination of glutathion (γ-Glu-Cys-Gly) induces the peptide link to be broken and a cyclization with the formation of lactone to occur.A second deamination takes place on the cysteinyl residue released and allows the formation of a thiiran by intramolecular cyclization with the thiol group.The formation of thiiran was also observed with oxidized glutathion which has an S-S bridge.Finally, the formation of nitrosamines was detected by 15N-NMR during the reaction of sodium nitrite with two commercial products available to the general public.

Renin inhibiting peptides with polar end groups

The present invention provides novel renin-inhibiting peptides having a noncleavable transition state insert corresponding to the 10,11- position of the renin substrate (angiotensinogen) and a polyhydroxy-substituted alkyl moiety bonded directly through carbon or nitrogen to the N-terminus. Such inhibitors are useful for the diagnosis and control of renin-dependent hypertension and other related diseases.