102522-48-5

Usage

Uses

Used in Pharmaceutical Industry:
N-[2-Hydroxy-1,1-bis(hydroxymethyl)ethyl]carbamic Acid Benzyl Ester is used as an intermediate for the preparation of glycocluster peptides. These peptides are essential in the development of drugs targeting various diseases, including cancer, due to their ability to modulate cellular interactions and signaling pathways.
Used in Chemical Synthesis:
As a carbamic acid derivative, N-[2-Hydroxy-1,1-bis(hydroxymethyl)ethyl]carbamic Acid Benzyl Ester can be utilized in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure allows for further functionalization and modification to create novel molecules with specific properties and applications.
Used in Research and Development:
N-[2-Hydroxy-1,1-bis(hydroxyMethyl)ethyl]carbaMic Acid Benzyl Ester serves as a valuable research tool for scientists and researchers working on the development of new drugs, materials, and chemical processes. Its unique structure and reactivity make it an interesting candidate for exploring new reaction pathways and understanding the underlying mechanisms of various chemical transformations.

Upstream product

• 1125824-87-4 C₁₉H₂₁NO₅ 
• 501-53-1 benzyl chloroformate 
• 77-86-1 2-amino-2-hydroxymethyl-1,3-propanediol 

Downstream Products

• 1228151-32-3 C₅₄H₅₃NO₁₁ 
• 69661-83-2 bis(ferrocenylmethyl)ether 
• 873070-03-2 N-Cbz-bis(hydroxymethyl)(ferrocene-methylene-oxymethyl)aminomethane 
• 873070-04-3 N-Cbz-bis(ferrocene-methylene-oxymethyl)-(hydroxymethyl)aminomethane 
• 151753-73-0 Acetic acid (2R,3S,4S,5R,6R)-3,5-diacetoxy-2-acetoxymethyl-6-[2-acetoxymethyl-2-benzyloxycarbonylamino-3-((2R,3R,4S,5S,6R)-3,4,5-triacetoxy-6-acetoxymethyl-tetrahydro-pyran-2-yloxy)-propoxy]-tetrahydro-pyran-4-yl ester 
• 151734-50-8 2-(benzyloxycarbonylamino)-3-hydroxy-2-(hydroxymethyl)propyl acetate 
• 420107-88-6 N-(benzyloxycarbonyl)-N'-heptadecylcarbamoyloxymethylbis[O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl)hydroxymethyl]aminomethane 
• 420107-87-5 N-(benzyloxycarbonyl)-N'-undecylcarbamoyloxymethylbis[O-(2,3,4,6-tetra-O-acetyl-β-D-galactopyranozyl)hydroxymethyl]aminomethane 
• 420107-83-1 5-N-(benzyloxycarbonyl)amino-5-N'-1H,1H,2H,2H-perfluorodecylcarbamoyloxymethyl-2,2-dimethyl-1,3-dioxane 
• 420107-86-4 N-(benzyloxycarbonyl)-N'-1H,1H,2H,2H-perfluorodecylcarbamoyloxymethylbis(hydroxymethyl)aminomethane 
• 420107-82-0 5-N-(benzyloxycarbonyl)amino-5-N'-heptadecylcarbamoyloxymethyl-2,2-dimethyl-1,3-dioxane 
• 420107-85-3 N-(benzyloxycarbonyl)-N'-heptadecylcarbamoyloxymethylbis(hydroxymethyl)aminomethane 
• 420107-84-2 N-(benzyloxycarbonyl)-N'-undecylcarbamoyloxymethylbis(hydroxymethyl)aminomethane 

Relevant academic research and scientific papers

A METHOD FOR THE PREPARATION OF FINGOLIMOD

The invention relates to a method of preparation of 2-amino-2-[2-(4-octylphenyl)- ethyl]propane-1,3-diol (I), comprising opening of the aziridine ring of the intermediates (LVI) by the treatment with organometallic compounds, preferably the Grignard reage

Saccharide-modified nanodiamond conjugates for the efficient detection and removal of pathogenic bacteria

The detection and removal of bacteria, such as E. coli in aqueous environments by using safe and readily available means is of high importance. Here we report on the synthesis of nanodiamonds (ND) covalently modified with specific carbohydrates (glyco-ND) for the precipitation of type 1 fimbriated uropathogenic E. coli in solution by mechanically stable agglutination. The surface of the diamond nanoparticles was modified by using a Diels-Alder reaction followed by the covalent grafting of the respective glycosides. The resulting glyco-ND samples are fully dispersible in aqueous media and show a surface loading of typically 0.1 mmol g-1. To probe the adhesive properties of various ND samples we have developed a new sandwich assay employing layers of two bacterial strains in an array format. Agglutination experiments in solution were used to distinguish unspecific interactions of glyco-ND with bacteria from specific ones. Two types of precipitates in solution were observed and characterized in detail by light and electron microscopy. Only by specific interactions mechanically stable agglutinates were formed. Bacteria could be removed from water by filtration of these stable agglutinates through 10 μm pore-size filters and the ND conjugate could eventually be recovered by addition of the appropriate carbohydrate. The application of glycosylated ND allows versatile and facile detection of bacteria and their efficient removal by using an environmentally and biomedically benign material. Copyright

Truly catalytic and chemoselective cleavage of benzylidene acetal with phosphomolybdic acid supported on silica gel

Phosphomolybdic acid supported on silica gel provides a truly catalytic method for the chemoselective cleavage of benzylidene acetals having sensitive functional groups under mild conditions. It is easy to perform on large scale owing to minimal catalyst loading (0.5 mol-%). Several sensitive functional groups such as TBDPS ether, -OMs, -OAc, allyl ether, N-Boc, N-Fmoc and N-Cbz are stable under the reaction conditions. In addition, benzylidene acetal is selectively cleaved in the presence of isopropylidene ketal. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

A new triferrocenyl-tris(hydroxymethyl)aminomethane derivative as a highly sensitive electrochemical marker of biomolecules: Application to the labelling of PNA monomers and their electrochemical characterization

We have designed and synthesised a new organometallic molecule containing three ferrocene groups for use as a highly sensitive electrochemical marker in biological assays. This trisferrocene derivative was conjugated to different PNA monomers, and the ele

SYNTHESIS OF ORGANOMETALLIC MOLECULES THAT CAN BE USED AS MARKERS OF ORGANIC SUBSTANCES

The present invention concerns compounds of general formula (I). These products are preferably used as labels of biomolecules (for example: nucleic acids, oligonucleotides, PNAs, peptides, proteins, steroids etc.) mainly used in the field of diagnostics.

Synthesis and study of the behavior of glycosylated gemini surfactants in aqueous media

The work reported herein deals with the synthesis and physico-chemical studies of a new kind of glycosylated non-ionic gemini surfactants. These compounds derive from tris(hydroxymethyl)aminomethane and bear hydro- or perfluorocarbon tails. The chemical structures of the spacer arm and hydrophobic tails were adjusted in order to specify their impact on the gemini surfactant behavior in aqueous media. The supramolecular systems they form were studied by TEM after negative staining. The length and the rigidity of the spacer arm seem to play a key role in the aggregation behavior of these surfactants in water. With the appropriate modifications, the formation of premicellar associations, micelles, vesicles or various aggregates can be observed.

A Convergent Synthesis of Carbohydrate-Containing Dendimers

The synthesis of carbohydrate-containing dendrimers has been achieved by a convergent grwoth approach.The synthetic strategy involves: 1) the synthesis of the triglucosylated derivative of tris(hydroxymethyl)methylamine (TRIS), 2) the introduction of a glycine-derived spacer and 3,3'-iminodipropionic acid derived branching units on to the TRIS derivative by amide bond formation, 3) condensation of the above saccharide-containing dendrons with a trifunctional 1,3,5-benzenetricarbonyl derivative, used as the core, by formation of amide bonds, and 4) deprotection of the saccharide units.A 9-mer and an 18-mer, carrying nine and eighteen saccharide units at the periphery, respectively, have been synthesized, in high yields at each step, by this synthetic strategy.By a variety of chromatographic and spectroscopic techniques, the dendrimers were shown to be structurally homogeneous, monodisperse, and error-free at all steps in their growth.These investigations were complemented by molecular modeling studies on the dendrimers.The presence of slightly distorted C3 symmetry was noted in both the 9-mer and the 18-mer. - Keywords: carbohydrates; cluster glucosides; convergent syntheses; dendrimers; neoglycoconjugates

Synthesis of polymerizable glycolipids derived from Tris (hydroxymethyl) aminomethane: Preparation of polymerized micelles

We have synthesized a series of new polymerizable glycolipids derived from Tris(hydroxymethyl) aminomethane (TRIS). Galactosylation of TRIS was performed in good yield by means of ultrasounds. Polymerization of 11-N-acrylamido-N-Tris(β-D-galactopyranosyl